Literature DB >> 26220959

FermiKit: assembly-based variant calling for Illumina resequencing data.

Heng Li1.   

Abstract

UNLABELLED: FermiKit is a variant calling pipeline for Illumina whole-genome germline data. It de novo assembles short reads and then maps the assembly against a reference genome to call SNPs, short insertions/deletions and structural variations. FermiKit takes about one day to assemble 30-fold human whole-genome data on a modern 16-core server with 85 GB RAM at the peak, and calls variants in half an hour to an accuracy comparable to the current practice. FermiKit assembly is a reduced representation of raw data while retaining most of the original information.
AVAILABILITY AND IMPLEMENTATION: https://github.com/lh3/fermikit CONTACT: hengli@broadinstitute.org.
© The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

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Year:  2015        PMID: 26220959      PMCID: PMC4757955          DOI: 10.1093/bioinformatics/btv440

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  11 in total

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6.  Structural variant identification and characterization.

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10.  ScanIndel: a hybrid framework for indel detection via gapped alignment, split reads and de novo assembly.

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