Wan-Ping Lee
Molecular Biology · 2012–2017
A researcher in the Science corpus: 5 papers; trusts 5 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 75 citations into it
- Genetics — 67 citations into it
- Artificial Intelligence — 9 citations into it
- Computational Biology & Bioinformatics — 6 citations into it
Whom Wan-Ping Lee trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Heng Li
- Temple F. Smith
- Michael Farrar
- Ruiqiang Li
- Andrzej Wozniak
- William R. Pearson
- Michael S. Waterman
- Mengyao Zhao
- M. Burrows
- Ben Langmead
Who trusts Wan-Ping Lee overall
Papers from Wan-Ping Lee's perspective
Ordered by how strongly the researchers Wan-Ping Lee trusts endorse each paper. Same corpus, a different order for every researcher.
- Identification of common molecular subsequences.
- SOAP: short oligonucleotide alignment program (Bioinform.)
- The Diploid Genome Sequence of an Individual Human (PLoS Biology)
- Exome sequencing as a tool for Mendelian disease gene discovery
- A Block-sorting Lossless Data Compression Algorithm
- SOAP2: an improved ultrafast tool for short read alignment (Bioinform.)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- Striped Smith-Waterman speeds database searches six times over other SIMD implementations (Bioinform.)
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
- Using video-oriented instructions to speed up sequence comparison
Their papers
- A global reference for human genetic variation (2015) — 16,925 citations
- Multi-platform discovery of haplotype-resolved structural variation in human genomes (2017) — 796 citations
- SSW Library: An SIMD Smith-Waterman C/C++ Library for Use in Genomic Applications (2012) — 246 citations
- MOSAIK: A Hash-Based Algorithm for Accurate Next-Generation Sequencing Short-Read Mapping (2013) — 295 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations