Lei M. Li

发表

MUREN: a robust and multi-reference approach of RNA-seq transcript normalization

Yance Feng, Lei M. Li, Yance Feng, 2021, BMC Bioinform..

BAUM: A DNA Assembler by Adaptive Unique Mapping and Local Overlap-Layout-Consensus

Lei M. Li, Anqi Wang, Zheng Li, 2016, 1609.03073.

DNA SEQUENCING AND PARAMETRIC DECONVOLUTION

Lei M. Li, 2003 .

An adaptive decorrelation method removes Illumina DNA base-calling errors caused by crosstalk between adjacent clusters

Lei M. Li, Anqi Wang, Bo Wang, 2017, Scientific reports.

Achieving Accurate and Fast Base-calling by a Block Model of the Illumina Sequencing Data

Bo Wang, Lei M. Li, Lin Wan, 2015 .

Accuracy Assessment of Consensus Sequence from Shotgun Sequencing

Lei M. Li, Lei M. Li, 2011, Handbook of Statistical Bioinformatics.

Estimating Phred scores of Illumina base calls by logistic regression and sparse modeling

Lei M. Li, Bo Wang, Sheng Zhang, 2017, BMC Bioinformatics.

A model-based approach to selection of tag SNPs

Fengzhu Sun, Pierre Nicolas, Lei M. Li, 2006, BMC Bioinformatics.

BAUM: improving genome assembly by adaptive unique mapping and local overlap‐layout‐consensus approach

Zheng Li, Lei M. Li, Anqi Wang, 2018, Bioinform..

SEME: A Fast Mapper of Illumina Sequencing Reads with Statistical Evaluation

Anqi Wang, Lei M. Li, Shijian Chen, 2013, RECOMB.

A model-based approach to selection of tag SNPs

Lei M. Li, Fengzhu Sun, P. Nicolas, 2006, BMC Bioinformatics.

SEME: A Fast Mapper of Illumina Sequencing Reads with Statistical Evaluation

Lei M. Li, Anqi Wang, Shijian Chen, 2013, RECOMB.

HAPLOWSER: a whole-genome haplotype browser for personal genome and metagenome

Lei M. Li, M. Waterman, Lei M. Li, 2009, Bioinform..

Estimating Phred scores of Illumina base calls by logistic regression and sparse modeling

Bo Wang, Lin Wan, Sheng Zhang, 2017, BMC Bioinformatics.