ppBAM: ProteinPaint BAM track for read alignment visualization and variant genotyping.
Where this comes from
- Record sourced from PubMed, PMID 37140547.
- Also identified by DOI 10.1093/bioinformatics/btad300 and PMC identifier 10182850.
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Abstract
ProteinPaint BAM track (ppBAM) is designed to assist variant review for cancer research and clinical genomics. With performant server-side computing and rendering, ppBAM supports on-the-fly variant genotyping of thousands of reads using Smith-Waterman alignment. To better visualize support for complex variants, reads are realigned against the mutated reference sequence using ClustalO. ppBAM also supports the BAM slicing API of the NCI Genomic Data Commons (GDC) portal, letting researchers conveniently examine genomic details of vast amounts of cancer sequencing data and reinterpret variant calls. BAM track examples, tutorial, and GDC file access links are available at https://proteinpaint.stjude.org/bam/. Source code is available at https://github.com/stjude/proteinpaint.
Medical subject headings
- Software
- Genomics