Nils Homer
Molecular Biology · 2008–2015
A researcher in the Science corpus: 7 papers; trusts 31 researchers and is trusted by 31 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 79 citations into it; #1,445 of 17,773 by trust here, #296 by citations
- Genetics — 53 citations into it; #1,556 of 6,854 by trust here, #35 by citations
- Artificial Intelligence — 14 citations into it; #6,764 of 35,345 by trust here, #1,211 by citations
- Ecology — 7 citations into it
- Computational Biology & Bioinformatics — 6 citations into it
Whom Nils Homer trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- W. James Kent
- Temple F. Smith
- Ruiqiang Li
- Ben Langmead
- Heng Li
- Michael Farrar
- Michael S. Waterman
- Zemin Ning
- Paolo Ferragina
- Stefan Kurtz
Who trusts Nils Homer overall
- Reza Shokri
- Alicia Oshlack
- Computational Pan-Genomics Consortium
- Congzheng Song
- Michael Backes
- Ahmed Salem
- Heng Li
- Cynthia Dwork
- Milad Nasr
- Fei Yu
Papers from Nils Homer's perspective
Ordered by how strongly the researchers Nils Homer trusts endorse each paper. Same corpus, a different order for every researcher.
- Identification of common molecular subsequences.
- BLAT--the BLAST-like alignment tool. (Genome Research)
- SOAP: short oligonucleotide alignment program (Bioinform.)
- Whole-genome re-sequencing. (Current Opinion in Genetics and Development)
- Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
- The human genome browser at UCSC.
- A Block-sorting Lossless Data Compression Algorithm
- Opportunistic data structures with applications
- SSAHA: a fast search method for large DNA databases. (Genome Research)
- Versatile and open software for comparing large genomes (Genome Biology)
Their papers
- The Sequence Alignment/Map format and SAMtools (2009) — 56,954 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- BFAST: An Alignment Tool for Large Scale Genome Resequencing (2009) — 586 citations
- An integrated semiconductor device enabling non-optical genome sequencing (2011) — 2,133 citations
- A survey of sequence alignment algorithms for next-generation sequencing (2010) — 971 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
- Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays (2008) — 1,347 citations