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Li, Heng
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ResearcherID: D-9344-2011
URL: http://www.researcherid.com/rid/D-9344-2011
ORCID: http://orcid.org/0000-0003-4874-2874
My Institutions (more details)
Primary Institution:
Sub-org/Dept: Medical Population Genetics program
Past Institutions: Wellcome Trust Sanger Institute
My URLs: http://lh3lh3.users.sourceforge.net
 

Publication Groups

Joint/first author (24)

Contributing author (38)

 

This list contains papers that I have authored.

publication(s)  
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1.  Title: Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly
 Author(s): Schneider, V. A.; Graves-Lindsay, T.; Howe, K.; et al.
 Source: Genome Research Volume: 27 Issue: 5 Pages: 849-864 Published: 2017
 Times Cited: 4
 DOI: 10.1101/gr.213611.116
added
13-Jul-17
2.  Title: Single-cell whole-genome analyses by Linear Amplification via Transposon Insertion (LIANTI)
 Author(s): Chen, C. Y.; Xing, D.; Tan, L. Z.; et al.
 Source: Science Volume: 356 Issue: 6334 Pages: 189-194 Published: 2017
 Times Cited: 9
 DOI: 10.1126/science.aak9787
added
13-Jul-17
3.  Title: BGT: efficient and flexible genotype query across many samples
 Author(s): Li, H.
 Source: Bioinformatics Volume: 32 Issue: 4 Pages: 590-592 Published: 2016
 Times Cited: 6
 DOI: 10.1093/bioinformatics/btv613
added
12-Aug-16
4.  Title: Minimap and miniasm: fast mapping and de novo assembly for noisy long sequences
 Author(s): Li, H.
 Source: Bioinformatics Volume: 32 Issue: 14 Pages: 2103-2110 Published: 2016
 Times Cited: 24
 DOI: 10.1093/bioinformatics/btw152
added
25-Oct-16
5.  Title: The contribution of rare variation to prostate cancer heritability
 Author(s): Mancuso, N.; Rohland, N.; Rand, K. A.; et al.
 Source: Nature Genetics Volume: 48 Issue: 1 Pages: 30-+ Published: 2016
 Times Cited: 17
 DOI: 10.1038/ng.3446
added
25-Oct-16
6.  Title: A global reference for human genetic variation
 Author(s): Altshuler, D. M.; Durbin, R. M.; Abecasis, G. R.; et al.
 Source: Nature Volume: 526 Issue: 7571 Pages: 68-+ Published: 2015
 Times Cited: 1036
 DOI: 10.1038/nature15393
added
12-Aug-16
7.  Title: BFC: correcting Illumina sequencing errors
 Author(s): Li, H.
 Source: Bioinformatics Volume: 31 Issue: 17 Pages: 2885-2887 Published: 2015
 Times Cited: 21
 DOI: 10.1093/bioinformatics/btv290
added
12-Aug-16
8.  Title: Complete Genomes Reveal Signatures of Demographic and Genetic Declines in the Woolly Mammoth
 Author(s): Palkopoulou, E.; Mallick, S.; Skoglund, P.; et al.
 Source: Current Biology Volume: 25 Issue: 10 Pages: 1395-1400 Published: 2015
 Times Cited: 43
 DOI: 10.1016/j.cub.2015.04.007
added
12-Aug-16
9.  Title: FermiKit: assembly-based variant calling for Illumina resequencing data
 Author(s): Li, H.
 Source: Bioinformatics Volume: 31 Issue: 22 Pages: 3694-3696 Published: 2015
 Times Cited: 8
 DOI: 10.1093/bioinformatics/btv440
added
12-Aug-16
10.  Title: No evidence that selection has been less effective at removing deleterious mutations in Europeans than in Africans
 Author(s): Do, R.; Balick, D.; Li, H.; et al.
 Source: Nature Genetics Volume: 47 Issue: 2 Pages: 126-131 Published: 2015
 Times Cited: 47
 DOI: 10.1038/ng.3186
added
12-Aug-16
publication(s)  
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