Search Results - "Li, Heng"
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Minimap2: pairwise alignment for nucleotide sequences
Published in Bioinformatics (15-09-2018)“…Abstract Motivation Recent advances in sequencing technologies promise ultra-long reads of ∼100 kb in average, full-length mRNA or cDNA reads in high…”
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New strategies to improve minimap2 alignment accuracy
Published in Bioinformatics (07-12-2021)“…Abstract Summary We present several recent improvements to minimap2, a versatile pairwise aligner for nucleotide sequences. Now minimap2 v2.22 can more…”
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Minimap and miniasm: fast mapping and de novo assembly for noisy long sequences
Published in Bioinformatics (Oxford, England) (15-07-2016)“…Single Molecule Real-Time (SMRT) sequencing technology and Oxford Nanopore technologies (ONT) produce reads over 10 kb in length, which have enabled…”
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A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data
Published in Bioinformatics (01-11-2011)“…Motivation: Most existing methods for DNA sequence analysis rely on accurate sequences or genotypes. However, in applications of the next-generation sequencing…”
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BFC: correcting Illumina sequencing errors
Published in Bioinformatics (01-09-2015)“…BFC is a free, fast and easy-to-use sequencing error corrector designed for Illumina short reads. It uses a non-greedy algorithm but still maintains a speed…”
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Tabix: fast retrieval of sequence features from generic TAB-delimited files
Published in Bioinformatics (Oxford, England) (01-03-2011)“…Tabix is the first generic tool that indexes position sorted files in TAB-delimited formats such as GFF, BED, PSL, SAM and SQL export, and quickly retrieves…”
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Improving SNP discovery by base alignment quality
Published in Bioinformatics (15-04-2011)“…I propose a new application of profile Hidden Markov Models in the area of SNP discovery from resequencing data, to greatly reduce false SNP calls caused by…”
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Toward better understanding of artifacts in variant calling from high-coverage samples
Published in Bioinformatics (Oxford, England) (15-10-2014)“…Whole-genome high-coverage sequencing has been widely used for personal and cancer genomics as well as in various research areas. However, in the lack of an…”
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FermiKit: assembly-based variant calling for Illumina resequencing data
Published in Bioinformatics (Oxford, England) (15-11-2015)“…FermiKit is a variant calling pipeline for Illumina whole-genome germline data. It de novo assembles short reads and then maps the assembly against a reference…”
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Tough Self‐Healing Elastomers by Molecular Enforced Integration of Covalent and Reversible Networks
Published in Advanced materials (Weinheim) (01-10-2017)“…Self‐healing polymers crosslinked by solely reversible bonds are intrinsically weaker than common covalently crosslinked networks. Introducing covalent…”
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Invalidity of, and alternative to, the linear quadratic model as a predictive model for postirradiation cell survival
Published in Cancer science (01-07-2023)“…The linear quadratic (LQ) model has been the dominant tool in preclinical radiobiological modeling of cell survival as a function of dose. However, as a…”
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Ultra‐High Performance Amorphous Ga2O3 Photodetector Arrays for Solar‐Blind Imaging
Published in Advanced science (01-10-2021)“…The growing demand for scalable solar‐blind image sensors with remarkable photosensitive properties has stimulated the research on more advanced solar‐blind…”
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Biological effectiveness and relative biological effectiveness of ion beams for in‐vitro cell irradiation
Published in Cancer science (01-08-2022)“…Biological effectiveness and relative biological effectiveness are critical for proton and ion beam radiotherapy. However, the relationship between the two…”
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Exploring single-sample SNP and INDEL calling with whole-genome de novo assembly
Published in Bioinformatics (15-07-2012)“…Eugene Myers in his string graph paper suggested that in a string graph or equivalently a unitig graph, any path spells a valid assembly. As a string/unitig…”
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Inference of human population history from individual whole-genome sequences
Published in Nature (London) (28-07-2011)“…Human population in the genes The history of human population size is important to understanding human evolution. Heng Li and Richard Durbin use complete…”
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Fast and accurate long-read alignment with Burrows–Wheeler transform
Published in Bioinformatics (01-03-2010)“…Motivation: Many programs for aligning short sequencing reads to a reference genome have been developed in the last 2 years. Most of them are very efficient…”
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Fast and accurate short read alignment with Burrows–Wheeler transform
Published in Bioinformatics (15-07-2009)“…Motivation: The enormous amount of short reads generated by the new DNA sequencing technologies call for the development of fast and accurate read alignment…”
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Evolutionary history of Coleoptera revealed by extensive sampling of genes and species
Published in Nature communications (15-01-2018)“…Beetles (Coleoptera) are the most diverse and species-rich group of insects, and a robust, time-calibrated phylogeny is fundamental to understanding…”
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The design and construction of reference pangenome graphs with minigraph
Published in Genome Biology (16-10-2020)“…The recent advances in sequencing technologies enable the assembly of individual genomes to the quality of the reference genome. How to integrate multiple…”
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Deep learning of subsurface flow via theory-guided neural network
Published in Journal of hydrology (Amsterdam) (01-05-2020)“…•TgNN model trained with data while being guided by theory of the underlying problem.•TgNN achieves better predictability, reliability, and generalizability…”
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