Nils W. Homer, Ph.D.

Affiliations: 
2010 University of California, Los Angeles, Los Angeles, CA 
Area:
bioinformatics; computational biology; machine learning
Google:
"Nils Homer"

Parents

Sign in to add mentor
Eleazar Eskin grad student 2010 UCLA
 (Computational Challenges in Genomic Analysis for the Discovery of the Genetic Basis of Human Disease.)
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Snedecor J, Fennell T, Stadick S, et al. (2022) Fast and accurate kinship estimation using sparse SNPs in relatively large database searches. Forensic Science International. Genetics. 61: 102769
Clark MJ, Homer N, O'Connor BD, et al. (2018) Correction: U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line. Plos Genetics. 14: e1007392
Brownstein CA, Beggs AH, Homer N, et al. (2014) An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge. Genome Biology. 15: R53
Rothberg JM, Hinz W, Rearick TM, et al. (2011) An integrated semiconductor device enabling non-optical genome sequencing. Nature. 475: 348-52
Homer N, Nelson SF. (2010) Improved variant discovery through local re-alignment of short-read next-generation sequencing data using SRMA. Genome Biology. 11: R99
Homer N, Nelson SF, Merriman B. (2010) Local alignment of generalized k-base encoded DNA sequence. Bmc Bioinformatics. 11: 347
Li H, Homer N. (2010) A survey of sequence alignment algorithms for next-generation sequencing. Briefings in Bioinformatics. 11: 473-483
Clark MJ, Homer N, O'Connor BD, et al. (2010) U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line. Plos Genetics. 6: e1000832
Lee H, O'Connor BD, Merriman B, et al. (2009) Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing. Bmc Genomics. 10: 646
Homer N, Merriman B, Nelson SF. (2009) BFAST: an alignment tool for large scale genome resequencing. Plos One. 4
See more...