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bowtie.debian.yaml
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identifiers:
- biotools: bowtie
- doi: 10.1186/gb-2009-10-3-r25
- debian: bowtie
- bioconda: bowtie
- scicrunch: SCR_005476
- omictools: OMICS_00653
homepage: http://bowtie-bio.sourceforge.net/
summary: Ultrafast memory-efficient short read aligner
description: >
This package addresses the problem to interpret the results from the
latest (2010) DNA sequencing technologies. Those will yield fairly
short stretches and those cannot be interpreted directly. It is the
challenge for tools like Bowtie to give a chromosomal location to the
short stretches of DNA sequenced per run.
.
Bowtie aligns short DNA sequences (reads) to the human genome at a rate
of over 25 million 35-bp reads per hour. Bowtie indexes the genome with
a Burrows-Wheeler index to keep its memory footprint small: typically
about 2.2 GB for the human genome (2.9 GB for paired-end).
version: 1.2.3
edam:
version: unknown
topics:
- Genomics
scopes:
- name: summary
function:
- Genome indexing
- Sequence alignment generation
input:
- data: Nucleic acid sequence (raw)
formats:
- FASTA
- FASTQ
output:
- data: Sequence alignment (nucleic acid)
formats:
- SAM
- name: bowtie-build
function:
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input:
- data: Nucleic acid sequence (raw)
formats:
- FASTA
output:
- data: Genome index
formats:
- Bowtie index format EBWT
- Bowtie long index format EBTWL
- name: bowtie-inspect
function:
- Sequence retrieval
- Metadata retrieval
- Data index analysis
input:
- data: Genome index
formats:
- Bowtie index format EBWT
- Bowtie long index format EBTWL
output:
- data: Nucleic acid sequence (raw)
formats:
- FASTA
- plain text format (unformatted)
- name: bowtie
function:
- Sequence database search (by sequence using word-based methods)
- Sequence alignment generation
input:
- data: Genome index
- data: Nucleic acid sequence (raw)
formats:
- plain text format (unformatted)
- FASTA
- FASTQ
output:
- data: Sequence alignment (nucleic acid)
- data: Sequence alignment report
formats:
- SAM
- Bowtie alignment report format