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Li, Heng
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ResearcherID: D-9344-2011
URL: http://www.researcherid.com/rid/D-9344-2011
Publons: https://publons.com/a/1331856
ORCID: http://orcid.org/0000-0003-4874-2874
My Institutions (more details)
Primary Institution:
Sub-org/Dept: Biomedical Informatics; Biostatistics and Computational Biology
Role:
Past Institutions: Wellcome Trust Sanger Institute; Broad Institute
My URLs: http://www.liheng.org
https://hlilab.github.io
 

Publication Groups

Joint/first author (26)

Contributing author (39)

 

This list contains papers that I have authored.

publication(s)  
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1.  Title: A synthetic-diploid benchmark for accurate variant-calling evaluation
 Author(s): Li, H.; Bloom, J. M.; Farjoun, Y.; et al.
 Source: Nature Methods Volume: 15 Issue: 8 Pages: 595-+ Published: 2018
 Times Cited: 0
 DOI: 10.1038/s41592-018-0054-7
added
08-Sep-18
2.  Title: Minimap2: pairwise alignment for nucleotide sequences
 Author(s): Li, H.
 Source: Bioinformatics Volume: 34 Issue: 18 Pages: 3094-3100 Published: 2018
 Times Cited: 8
 DOI: 10.1093/bioinformatics/bty191
added
17-Oct-18
3.  Title: Three-dimensional genome structures of single diploid human cells
 Author(s): Tan, L. Z.; Xing, D.; Chang, C. H.; et al.
 Source: Science Volume: 361 Issue: 6405 Pages: 924-928 Published: 2018
 Times Cited: 1
 DOI: 10.1126/science.aat5641
added
17-Sep-18
4.  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: 28
 DOI: 10.1101/gr.213611.116
added
13-Jul-17
5.  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: 33
 DOI: 10.1126/science.aak9787
added
13-Jul-17
6.  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: 8
 DOI: 10.1093/bioinformatics/btv613
added
12-Aug-16
7.  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: 62
 DOI: 10.1093/bioinformatics/btw152
added
25-Oct-16
8.  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: 28
 DOI: 10.1038/ng.3446
added
25-Oct-16
9.  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: 2021
 DOI: 10.1038/nature15393
added
12-Aug-16
10.  Title: BFC: correcting Illumina sequencing errors
 Author(s): Li, H.
 Source: Bioinformatics Volume: 31 Issue: 17 Pages: 2885-2887 Published: 2015
 Times Cited: 34
 DOI: 10.1093/bioinformatics/btv290
added
12-Aug-16
publication(s)  
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