William Stephen Pittard

Genetics · 2006–2013

A researcher in the Science corpus: 4 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 42 citations into it

Whom William Stephen Pittard trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Ryan E. Mills

Papers from William Stephen Pittard's perspective

Ordered by how strongly the researchers William Stephen Pittard trusts endorse each paper. Same corpus, a different order for every researcher.

1. Base-calling of automated sequencer traces using phred. I. Accuracy assessment.
2. Repbase update: a database and an electronic journal of repetitive elements. (Trends in Genetics)
3. The human genome browser at UCSC.
4. Fine-scale structural variation of the human genome (Nature Genetics)
5. Haplotype Variation and Linkage Disequilibrium in 313 Human Genes (Science)
6. High-resolution haplotype structure in the human genome (Nature Genetics)
7. Base-calling of automated sequencer traces using phred. II. Error probabilities.
8. Human Gene Mutation Database (HGMD®): 2003 update
9. Mapping copy number variation by population scale genome sequencing (Nature)
10. Rapid gene mapping in Caenorhabditis elegans using a high density polymorphism map (Nature Genetics)

Their papers

• An initial map of insertion and deletion (INDEL) variation in the human genome. (2006) — 678 citations
• Small insertions and deletions (INDELs) in human genomes. (2010) — 365 citations
• xMSanalyzer: automated pipeline for improved feature detection and downstream analysis of large-scale, non-targeted metabolomics data (2013) — 352 citations
• Natural genetic variation caused by small insertions and deletions in the human genome. (2011) — 272 citations