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arxiv: 1303.3997 · v2 · pith:FZSGG5B7new · submitted 2013-03-16 · 🧬 q-bio.GN

Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM

classification 🧬 q-bio.GN
keywords bwa-memreadssequencesequencesalgorithmaligningalignmentaligners
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Summary: BWA-MEM is a new alignment algorithm for aligning sequence reads or long query sequences against a large reference genome such as human. It automatically chooses between local and end-to-end alignments, supports paired-end reads and performs chimeric alignment. The algorithm is robust to sequencing errors and applicable to a wide range of sequence lengths from 70bp to a few megabases. For mapping 100bp sequences, BWA-MEM shows better performance than several state-of-art read aligners to date. Availability and implementation: BWA-MEM is implemented as a component of BWA, which is available at http://github.com/lh3/bwa. Contact: hengli@broadinstitute.org

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Cited by 3 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score.

  1. AirLift: A Fast and Comprehensive Technique for Remapping Alignments between Reference Genomes

    q-bio.GN 2019-12 conditional novelty 7.0

    AirLift remaps read alignments between similar reference genomes up to 27.4x faster than full re-mapping while maintaining high accuracy for SNP and INDEL variant calling as validated with GATK.

  2. Parse indexing for choosing pseudo-MEMs

    cs.DS 2026-05 unverdicted novelty 6.0

    Parse indexing enables safe choice and filtering of pseudo-MEMs for MEM searches without selecting k.

  3. Parse indexing for choosing pseudo-MEMs

    cs.DS 2026-05 unverdicted novelty 5.0

    The paper shows how parse indexing can select pseudo-MEMs that contain every MEM of length at least k while eliminating the need to choose k and the risk of discarding important matches.