BAM-matcher: A tool for rapid NGS sample matching

Bioinformatics

Volumn 32, Issue 17, 2016, Pages 2699-2701

  Wang, Paul P S ^a,b   Parker, Wendy T ^a,b,c   Branford, Susan ^a,c,d   Schreiber, Andreas W ^b,d  

^a Department of Genetics and Molecular Pathology ^*  (Australia)

^b CENTRE FOR CANCER BIOLOGY   (Australia)

^c UNIVERSITY OF SOUTH AUSTRALIA   (Australia)

^d UNIVERSITY OF ADELAIDE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

DNA SEQUENCE; GENOME; GENOTYPE; GENOTYPING TECHNIQUE; HIGH THROUGHPUT SEQUENCING; HUMAN; SEQUENCE ALIGNMENT; SOFTWARE;

GENOME; GENOTYPE; GENOTYPING TECHNIQUES; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, DNA; SOFTWARE;

EID: 84990890570     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btw239     Document Type: Conference Paper

References (5)

1. Garrison, E. and Marth, G. (2012) Haplotype-based variant detection from short-read sequencing. arXiv, 1207.3907 [q-bio.GN]
2. Grimm, E. et al. (2010) Blood bank safety practices: mislabeled samples and wrong blood in tube-A Q-probes analysis of 122 clinical laboratories. Arch. Pathol. Lab. Med., 134, 1108-1115
3. Koboldt, D.C. et al. (2010) Challenges of sequencing human genomes. Brief Bioinform., 11, 484-498
4. McKenna, A. et al. (2010) The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res., 20, 1297-1303
5. The 1000 Genomes Project Consortium (2012) An integrated map of genetic variation from 1, 092 human genomes. Nature, 491, 56-65