Heng Li

Orcid: 0000-0003-4874-2874

Affiliations:
  • Broad Institute of Harvard and MIT, Medical Population Genetics Program, Cambridge, MA, USA
  • Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK (former)
  • Chinese Academy of Sciences, Beijing Genomics Institute, China (former)


According to our database1, Heng Li authored at least 27 papers between 2006 and 2021.

Collaborative distances:
  • Dijkstra number2 of four.
  • Erdős number3 of four.

Timeline

Legend:

Book 
In proceedings 
Article 
PhD thesis 
Dataset
Other 

Links

Online presence:

On csauthors.net:

Bibliography

2021
Real-time mapping of nanopore raw signals.
Bioinform., 2021

Bedtk: finding interval overlap with implicit interval tree.
Bioinform., 2021

New strategies to improve minimap2 alignment accuracy.
Bioinform., 2021

2020
A haplotype-aware de novo assembly of related individuals using pedigree sequence graph.
Bioinform., 2020

2019
Identifying centromeric satellites with dna-brnn.
Bioinform., 2019

Efficient Architecture-Aware Acceleration of BWA-MEM for Multicore Systems.
Proceedings of the 2019 IEEE International Parallel and Distributed Processing Symposium, 2019

2016
Minimap and miniasm: fast mapping and de novo assembly for noisy long sequences.
Bioinform., 2016

BGT: efficient and flexible genotype query across many samples.
Bioinform., 2016

2015
FermiKit: assembly-based variant calling for Illumina resequencing data.
Bioinform., 2015

BFC: correcting Illumina sequencing errors.
Bioinform., 2015

2014
Fast construction of FM-index for long sequence reads.
Bioinform., 2014

Toward better understanding of artifacts in variant calling from high-coverage samples.
Bioinform., 2014

2012
Exploring single-sample SNP and INDEL calling with whole-genome <i>de novo</i> assembly.
Bioinform., 2012

2011
A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data.
Bioinform., 2011

Improving SNP discovery by base alignment quality.
Bioinform., 2011

Tabix: fast retrieval of sequence features from generic TAB-delimited files.
Bioinform., 2011

2010
Evolutionary Transients in the Rice Transcriptome.
Genom. Proteom. Bioinform., 2010

Fast and accurate long-read alignment with Burrows-Wheeler transform.
Bioinform., 2010

A survey of sequence alignment algorithms for next-generation sequencing.
Briefings Bioinform., 2010

2009
The Sequence Alignment/Map format and SAMtools.
Bioinform., 2009

Fast and accurate short read alignment with Burrows-Wheeler transform.
Bioinform., 2009

Detecting SNPs and estimating allele frequencies in clonal bacterial populations by sequencing pooled DNA.
Bioinform., 2009

2008
TreeFam: 2008 Update.
Nucleic Acids Res., 2008

2007
PigGIS: Pig Genomic Informatics System.
Nucleic Acids Res., 2007

Snap: an integrated SNP annotation platform.
Nucleic Acids Res., 2007

A cross-species alignment tool (<i>CAT</i>).
BMC Bioinform., 2007

2006
TreeFam: a curated database of phylogenetic trees of animal gene families.
Nucleic Acids Res., 2006


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