Genome instability-derived genes as a novel prognostic signature for lung adenocarcinoma

por Zhang, Xu, Lam, Tak-Wah, Ting, Hing-Fung
Publicado 2023

PnpProbs: a better multiple sequence alignment tool by better handling of guide trees

por Ye, Yongtao, Lam, Tak-Wah, Ting, Hing-Fung
Publicado 2016

A simple and economical method for improving whole genome alignment

por Mai, Huijun, Lam, Tak-Wah, Ting, Hing-Fung
Publicado 2017

Next generation sequencing has lower sequence coverage and poorer SNP-detection capability in the regulatory regions

por Wang, Weixin, Wei, Zhi, Lam, Tak-Wah, Wang, Junwen
Publicado 2011

Assembly-free discovery of human novel sequences using long reads

por Li, Qiuhui, Yan, Bin, Lam, Tak-Wah, Luo, Ruibang
Publicado 2022

Boosting variant-calling performance with multi-platform sequencing data using Clair3-MP

por Yu, Huijing, Zheng, Zhenxian, Su, Junhao, Lam, Tak-Wah, Luo, Ruibang
Publicado 2023

A multi-task convolutional deep neural network for variant calling in single molecule sequencing

por Luo, Ruibang, Sedlazeck, Fritz J., Lam, Tak-Wah, Schatz, Michael C.
Publicado 2019

RENET2: high-performance full-text gene–disease relation extraction with iterative training data expansion

por Su, Junhao, Wu, Ye, Ting, Hing-Fung, Lam, Tak-Wah, Luo, Ruibang
Publicado 2021

Clair3-trio: high-performance Nanopore long-read variant calling in family trios with trio-to-trio deep neural networks

por Su, Junhao, Zheng, Zhenxian, Ahmed, Syed Shakeel, Lam, Tak-Wah, Luo, Ruibang
Publicado 2022

Adjacent Nucleotide Dependence in ncRNA and Order-1 SCFG for ncRNA Identification

por Wong, Thomas K. F., Lam, Tak-Wah, Sung, Wing-Kin, Yiu, Siu-Ming
Publicado 2010

Local structural alignment of RNA with affine gap model

por King-Fung Wong, Thomas, Wing-Yan Cheung, Brenda, Lam, Tak-Wah, Yiu, Siu-Ming
Publicado 2011

CONNET: Accurate Genome Consensus in Assembling Nanopore Sequencing Data via Deep Learning

por Zhang, Yifan, Liu, Chi-Man, Leung, Henry C.M., Luo, Ruibang, Lam, Tak-Wah
Publicado 2020

Duet: SNP-assisted structural variant calling and phasing using Oxford nanopore sequencing

por Zhou, Yekai, Leung, Amy Wing-Sze, Ahmed, Syed Shakeel, Lam, Tak-Wah, Luo, Ruibang
Publicado 2022

Improving multiple sequence alignment by using better guide trees

por Zhan, Qing, Ye, Yongtao, Lam, Tak-Wah, Yiu, Siu-Ming, Wang, Yadong, Ting, Hing-Fung
Publicado 2015

MegaGTA: a sensitive and accurate metagenomic gene-targeted assembler using iterative de Bruijn graphs

por Li, Dinghua, Huang, Yukun, Leung, Chi-Ming, Luo, Ruibang, Ting, Hing-Fung, Lam, Tak-Wah
Publicado 2017

Building a Chinese pan-genome of 486 individuals

por Li, Qiuhui, Tian, Shilin, Yan, Bin, Liu, Chi Man, Lam, Tak-Wah, Li, Ruiqiang, Luo, Ruibang
Publicado 2021

SOAPsplice: Genome-Wide ab initio Detection of Splice Junctions from RNA-Seq Data

por Huang, Songbo, Zhang, Jinbo, Li, Ruiqiang, Zhang, Wenqian, He, Zengquan, Lam, Tak-Wah, Peng, Zhiyu, Yiu, Siu-Ming
Publicado 2011

BALSA: integrated secondary analysis for whole-genome and whole-exome sequencing, accelerated by GPU

por Luo, Ruibang, Wong, Yiu-Lun, Law, Wai-Chun, Lee, Lap-Kei, Cheung, Jeanno, Liu, Chi-Man, Lam, Tak-Wah
Publicado 2014

Transcriptome Analysis of Acute Phase Liver Graft Injury in Liver Transplantation

por Lee, Nikki P., Wu, Haiyang, Ng, Kevin T.P., Luo, Ruibang, Lam, Tak-Wah, Lo, Chung-Mau, Man, Kwan
Publicado 2018

BASE: a practical de novo assembler for large genomes using long NGS reads

por Liu, Binghang, Liu, Chi-Man, Li, Dinghua, Li, Yingrui, Ting, Hing-Fung, Yiu, Siu-Ming, Luo, Ruibang, Lam, Tak-Wah
Publicado 2016