Align sequence reads to reference sequences using the Bowtie 1
(bowtie
) and Bowtie 2
(bowtie2
) alignment functions. Bowtie 1 is
geared toward aligning relatively short reads (up to 50 bp). Bowtie 2 is
more suitable for reads longer than 50 bp and provides several benefits
including single- and paired-end reads support, local and end-to-end
alignment support, and gapped alignment with affine penalties.
bowtie | Map short reads to reference sequence using Burrows-Wheeler transform |
bowtiebuild | Generate index using Burrows-Wheeler transform |
bowtie2 | Map sequence reads to reference sequence |
bowtie2build | Create Bowtie 2 index files from reference sequences |
bowtie2inspect | Inspect Bowtie 2 index files |
bwaindex | Create BWA indices from reference sequence |
bwamem | Map sequence reads to reference genome using BWA |
align2cigar | Convert aligned sequences to corresponding signatures in CIGAR format |
cigar2align | Convert unaligned sequences to aligned sequences using signatures in CIGAR format |
BioMap | Contain sequence, quality, alignment, and mapping data |
Bowtie2AlignOptions | Options to map reads to reference sequence |
Bowtie2BuildOptions | Contain options to create Bowtie 2 index files from reference sequences |
Bowtie2InspectOptions | Contain options to inspect Bowtie 2 index files |
BWAIndexOptions | Option set for bwaindex |
BWAMEMOptions | Option set for bwamem |
Visualize NGS Data Using Genomics Viewer App
Use the Genomics Viewer app to view NGS alignment data for single nucleotide variation in cytochrome p450 gene.
Bioinformatics Toolbox Software Support Packages
Download and install Bioinformatics support packages for NGS workflows.