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 26 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

Bibliography

2021

Real-time mapping of nanopore raw signals.

[BibT_eX]

[DOI]

Bioinform., 2021

Bedtk: finding interval overlap with implicit interval tree.

[BibT_eX]

[DOI]

Heng Li

Jiazhen Rong

Bioinform., 2021

New strategies to improve minimap2 alignment accuracy.

[BibT_eX]

[DOI]

Heng Li

Bioinform., 2021

2020

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

[BibT_eX]

[DOI]

Bioinform., 2020

2019

Identifying centromeric satellites with dna-brnn.

[BibT_eX]

[DOI]

Heng Li

Bioinform., 2019

2016

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

[BibT_eX]

[DOI]

Heng Li

Bioinform., 2016

BGT: efficient and flexible genotype query across many samples.

[BibT_eX]

[DOI]

Heng Li

Bioinform., 2016

2015

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

[BibT_eX]

[DOI]

Heng Li

Bioinform., 2015

BFC: correcting Illumina sequencing errors.

[BibT_eX]

[DOI]

Heng Li

Bioinform., 2015

2014

Fast construction of FM-index for long sequence reads.

[BibT_eX]

[DOI]

Heng Li

Bioinform., 2014

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

[BibT_eX]

[DOI]

Heng Li

Bioinform., 2014

2012

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

[BibT_eX]

[DOI]

Heng Li

Bioinform., 2012

2011

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

[BibT_eX]

[DOI]

Heng Li

Bioinform., 2011

Improving SNP discovery by base alignment quality.

[BibT_eX]

[DOI]

Heng Li

Bioinform., 2011

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

[BibT_eX]

[DOI]

Heng Li

Bioinform., 2011

2010

Evolutionary Transients in the Rice Transcriptome.

[BibT_eX]

[DOI]

Genom. Proteom. Bioinform., 2010

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

[BibT_eX]

[DOI]

Heng Li

Richard Durbin

Bioinform., 2010

A survey of sequence alignment algorithms for next-generation sequencing.

[BibT_eX]

[DOI]

Heng Li

Nils Homer

Briefings Bioinform., 2010

2009

The Sequence Alignment/Map format and SAMtools.

[BibT_eX]

[DOI]

Bioinform., 2009

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

[BibT_eX]

[DOI]

Heng Li

Richard Durbin

Bioinform., 2009

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

[BibT_eX]

[DOI]

Bioinform., 2009

2008

TreeFam: 2008 Update.

[BibT_eX]

[DOI]

Lachlan James M. Coin

Nucleic Acids Res., 2008

2007

PigGIS: Pig Genomic Informatics System.

[BibT_eX]

[DOI]

Nucleic Acids Res., 2007

Snap: an integrated SNP annotation platform.

[BibT_eX]

[DOI]

Nucleic Acids Res., 2007

A cross-species alignment tool (<i>CAT</i>).

[BibT_eX]

[DOI]

BMC Bioinform., 2007

2006

TreeFam: a curated database of phylogenetic trees of animal gene families.

[BibT_eX]

[DOI]

Heng Li

Avril Coghlan

Jue Ruan

Lachlan James M. Coin

Nucleic Acids Res., 2006

Heng Li

Timeline

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