pregap4.desktop - 2.0.0+b11-2 ⚙ amd64
⚙ armhf
⚙ arm64
⚙ i386
⚙ ppc64el
⚙ s390x
---
Type: desktop-application
ID: pregap4.desktop
Package: staden
Name:
C: pregap4
Summary:
C: Staden pregap4 DNA preprocessor
Description:
en_GB: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
C: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
en_AU: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
it: >-
<p>Staden è un insieme completamente sviluppato di strumenti per assemblaggio (Gap4 e Gap5), modifica e analisi di sequenze
di DNA.</p>
<p>Gap4 effettua l'assemblaggio di sequenze, l'ordinamento di contigui basato su dati di coppie di letture,
l'unione di contigui basata sul confronto di sequenze, il controllo di assemblaggi, la ricerca di sequenze ripetute,
il suggerimento di esperimenti, l'analisi di coppie di letture e la modifica di contigui. Ha viste grafiche di contigui,
modelli, letture e tracce, tutte con scorrimento nel registro. Le funzioni di suggerimento di esperimenti e le ricerche
dell'editor di contigui usano valori di confidenza per calcolare la confidenza della sequenza di consenso e perciò
identificare solamente le posizioni che richiedono l'ispezione visiva delle tracce o dati aggiuntivi. Il risultato
è un tempo estremamente rapido e un consenso di accuratezza nota.</p>
<p>Pregap4 fornisce un'interfaccia utente grafica per impostare l'elaborazione necessaria per preparare dati
di tracce per l'assemblaggio o l'analisi e automatizza questi processi.</p>
<p>Trev è un visualizzatore e un editor rapido e flessibile per file di traccia ABI, ALF, SCF e ZTR.</p>
<p>Prefinish analizza assemblaggi di sequenze parzialmente completi e suggerisce l'insieme più efficiente di esperimenti
per aiutare a completare il progetto.</p>
<p>Tracediff e hetscan localizzano automaticamente mutazioni confrontando dati di tracce con tracce di riferimento. Annotano
le mutazioni trovate in modo che siano pronte per la visualizzazione in gap4.</p>
<p>Spin analizza sequenze di nucleotidi per trovare geni, siti di restrizione, motivi, ecc. Può effettuare traduzioni,
trovare frame di lettura aperti, contare i codoni, ecc. Molti risultati sono presentati graficamente e una finestra per
sequenza con scorrimento è collegata al cursore grafico. Spin inoltre confronta coppie di sequenze in molti modi. Ha un'analisi
a matrice di punti molto veloce, algoritmi di allineamento globale e locale più una finestra per sequenza con scorrimento
collegata ai tracciati grafici. Può confrontare acidi nucleici con acidi nucleici, proteine con proteine e proteine con
acidi nucleici.</p>
en: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
en_CA: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
Categories:
- Biology
- Science
Icon:
cached:
- name: staden_icon4bl.png
width: 64
height: 64
Launchable:
desktop-id:
- pregap4.desktop
gap4.desktop - 2.0.0+b11-2 ⚙ amd64
⚙ armhf
⚙ arm64
⚙ i386
⚙ ppc64el
⚙ s390x
---
Type: desktop-application
ID: gap4.desktop
Package: staden
Name:
C: gap4
Summary:
C: Staden gap4 assembly editor
Description:
en_GB: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
C: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
en_AU: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
it: >-
<p>Staden è un insieme completamente sviluppato di strumenti per assemblaggio (Gap4 e Gap5), modifica e analisi di sequenze
di DNA.</p>
<p>Gap4 effettua l'assemblaggio di sequenze, l'ordinamento di contigui basato su dati di coppie di letture,
l'unione di contigui basata sul confronto di sequenze, il controllo di assemblaggi, la ricerca di sequenze ripetute,
il suggerimento di esperimenti, l'analisi di coppie di letture e la modifica di contigui. Ha viste grafiche di contigui,
modelli, letture e tracce, tutte con scorrimento nel registro. Le funzioni di suggerimento di esperimenti e le ricerche
dell'editor di contigui usano valori di confidenza per calcolare la confidenza della sequenza di consenso e perciò
identificare solamente le posizioni che richiedono l'ispezione visiva delle tracce o dati aggiuntivi. Il risultato
è un tempo estremamente rapido e un consenso di accuratezza nota.</p>
<p>Pregap4 fornisce un'interfaccia utente grafica per impostare l'elaborazione necessaria per preparare dati
di tracce per l'assemblaggio o l'analisi e automatizza questi processi.</p>
<p>Trev è un visualizzatore e un editor rapido e flessibile per file di traccia ABI, ALF, SCF e ZTR.</p>
<p>Prefinish analizza assemblaggi di sequenze parzialmente completi e suggerisce l'insieme più efficiente di esperimenti
per aiutare a completare il progetto.</p>
<p>Tracediff e hetscan localizzano automaticamente mutazioni confrontando dati di tracce con tracce di riferimento. Annotano
le mutazioni trovate in modo che siano pronte per la visualizzazione in gap4.</p>
<p>Spin analizza sequenze di nucleotidi per trovare geni, siti di restrizione, motivi, ecc. Può effettuare traduzioni,
trovare frame di lettura aperti, contare i codoni, ecc. Molti risultati sono presentati graficamente e una finestra per
sequenza con scorrimento è collegata al cursore grafico. Spin inoltre confronta coppie di sequenze in molti modi. Ha un'analisi
a matrice di punti molto veloce, algoritmi di allineamento globale e locale più una finestra per sequenza con scorrimento
collegata ai tracciati grafici. Può confrontare acidi nucleici con acidi nucleici, proteine con proteine e proteine con
acidi nucleici.</p>
en: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
en_CA: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
Categories:
- Biology
- Science
Icon:
cached:
- name: staden_icon4bl.png
width: 64
height: 64
Launchable:
desktop-id:
- gap4.desktop
gap5.desktop - 2.0.0+b11-2 ⚙ amd64
⚙ armhf
⚙ arm64
⚙ i386
⚙ ppc64el
⚙ s390x
---
Type: desktop-application
ID: gap5.desktop
Package: staden
Name:
C: gap5
Summary:
C: Staden gap5 assembly editor
Description:
en_GB: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
C: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
en_AU: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
it: >-
<p>Staden è un insieme completamente sviluppato di strumenti per assemblaggio (Gap4 e Gap5), modifica e analisi di sequenze
di DNA.</p>
<p>Gap4 effettua l'assemblaggio di sequenze, l'ordinamento di contigui basato su dati di coppie di letture,
l'unione di contigui basata sul confronto di sequenze, il controllo di assemblaggi, la ricerca di sequenze ripetute,
il suggerimento di esperimenti, l'analisi di coppie di letture e la modifica di contigui. Ha viste grafiche di contigui,
modelli, letture e tracce, tutte con scorrimento nel registro. Le funzioni di suggerimento di esperimenti e le ricerche
dell'editor di contigui usano valori di confidenza per calcolare la confidenza della sequenza di consenso e perciò
identificare solamente le posizioni che richiedono l'ispezione visiva delle tracce o dati aggiuntivi. Il risultato
è un tempo estremamente rapido e un consenso di accuratezza nota.</p>
<p>Pregap4 fornisce un'interfaccia utente grafica per impostare l'elaborazione necessaria per preparare dati
di tracce per l'assemblaggio o l'analisi e automatizza questi processi.</p>
<p>Trev è un visualizzatore e un editor rapido e flessibile per file di traccia ABI, ALF, SCF e ZTR.</p>
<p>Prefinish analizza assemblaggi di sequenze parzialmente completi e suggerisce l'insieme più efficiente di esperimenti
per aiutare a completare il progetto.</p>
<p>Tracediff e hetscan localizzano automaticamente mutazioni confrontando dati di tracce con tracce di riferimento. Annotano
le mutazioni trovate in modo che siano pronte per la visualizzazione in gap4.</p>
<p>Spin analizza sequenze di nucleotidi per trovare geni, siti di restrizione, motivi, ecc. Può effettuare traduzioni,
trovare frame di lettura aperti, contare i codoni, ecc. Molti risultati sono presentati graficamente e una finestra per
sequenza con scorrimento è collegata al cursore grafico. Spin inoltre confronta coppie di sequenze in molti modi. Ha un'analisi
a matrice di punti molto veloce, algoritmi di allineamento globale e locale più una finestra per sequenza con scorrimento
collegata ai tracciati grafici. Può confrontare acidi nucleici con acidi nucleici, proteine con proteine e proteine con
acidi nucleici.</p>
en: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
en_CA: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
Categories:
- Biology
- Science
Icon:
cached:
- name: staden_icon4bl.png
width: 64
height: 64
Launchable:
desktop-id:
- gap5.desktop
trev.desktop - 2.0.0+b11-2 ⚙ amd64
⚙ armhf
⚙ arm64
⚙ i386
⚙ ppc64el
⚙ s390x
---
Type: desktop-application
ID: trev.desktop
Package: staden
Name:
C: trev
Summary:
C: Staden trev program
Description:
en_GB: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
C: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
en_AU: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
it: >-
<p>Staden è un insieme completamente sviluppato di strumenti per assemblaggio (Gap4 e Gap5), modifica e analisi di sequenze
di DNA.</p>
<p>Gap4 effettua l'assemblaggio di sequenze, l'ordinamento di contigui basato su dati di coppie di letture,
l'unione di contigui basata sul confronto di sequenze, il controllo di assemblaggi, la ricerca di sequenze ripetute,
il suggerimento di esperimenti, l'analisi di coppie di letture e la modifica di contigui. Ha viste grafiche di contigui,
modelli, letture e tracce, tutte con scorrimento nel registro. Le funzioni di suggerimento di esperimenti e le ricerche
dell'editor di contigui usano valori di confidenza per calcolare la confidenza della sequenza di consenso e perciò
identificare solamente le posizioni che richiedono l'ispezione visiva delle tracce o dati aggiuntivi. Il risultato
è un tempo estremamente rapido e un consenso di accuratezza nota.</p>
<p>Pregap4 fornisce un'interfaccia utente grafica per impostare l'elaborazione necessaria per preparare dati
di tracce per l'assemblaggio o l'analisi e automatizza questi processi.</p>
<p>Trev è un visualizzatore e un editor rapido e flessibile per file di traccia ABI, ALF, SCF e ZTR.</p>
<p>Prefinish analizza assemblaggi di sequenze parzialmente completi e suggerisce l'insieme più efficiente di esperimenti
per aiutare a completare il progetto.</p>
<p>Tracediff e hetscan localizzano automaticamente mutazioni confrontando dati di tracce con tracce di riferimento. Annotano
le mutazioni trovate in modo che siano pronte per la visualizzazione in gap4.</p>
<p>Spin analizza sequenze di nucleotidi per trovare geni, siti di restrizione, motivi, ecc. Può effettuare traduzioni,
trovare frame di lettura aperti, contare i codoni, ecc. Molti risultati sono presentati graficamente e una finestra per
sequenza con scorrimento è collegata al cursore grafico. Spin inoltre confronta coppie di sequenze in molti modi. Ha un'analisi
a matrice di punti molto veloce, algoritmi di allineamento globale e locale più una finestra per sequenza con scorrimento
collegata ai tracciati grafici. Può confrontare acidi nucleici con acidi nucleici, proteine con proteine e proteine con
acidi nucleici.</p>
en: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
en_CA: >-
<p>Staden is a fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and analysis tools (Spin).</p>
<p>Gap4 performs sequence assembly, contig ordering based on read pair data, contig joining based on sequence comparisons,
assembly checking, repeat searching, experiment suggestion, read pair analysis and contig editing. It has graphical views
of contigs, templates, readings and traces which all scroll in register. Contig editor searches and experiment suggestion
routines use confidence values to calculate the confidence of the consensus sequence and hence identify only places requiring
visual trace inspection or extra data. The result is extremely rapid finishing and a consensus of known accuracy.</p>
<p>Pregap4 provides a graphical user interface to set up the processing required to prepare trace data for assembly or
analysis, and automates these processes.</p>
<p>Trev is a rapid and flexible viewer and editor for ABI, ALF, SCF and ZTR trace files.</p>
<p>Prefinish analyses partially completed sequence assemblies and suggests the most efficient set of experiments to help
finish the project.</p>
<p>Tracediff and hetscan automatically locate mutations by comparing trace data against reference traces. They annotate
the mutations found ready for viewing in gap4.</p>
<p>Spin analyses nucleotide sequences to find genes, restriction sites, motifs, etc. It can perform translations, find
open reading frames, count codons, etc. Many results are presented graphically and a sliding sequence window is linked
to the graphics cursor. Spin also compares pairs of sequences in many ways. It has very rapid dot matrix analysis, global
and local alignment algorithms, plus a sliding sequence window linked to the graphical plots. It can compare nucleic acid
against nucleic acid, protein against protein, and protein against nucleic acid.</p>
Categories:
- Biology
- Science
Icon:
cached:
- name: staden_icon4bl.png
width: 64
height: 64
Launchable:
desktop-id:
- trev.desktop