Ernest T Lam
Ernest T Lam
Epic Sciences
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Cited by
Cited by
Genome mapping on nanochannel arrays for structural variation analysis and sequence assembly
ET Lam, A Hastie, C Lin, D Ehrlich, SK Das, MD Austin, P Deshpande, ...
Nature biotechnology 30 (8), 771-776, 2012
Multi-platform discovery of haplotype-resolved structural variation in human genomes
MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ...
Nature communications 10 (1), 1-16, 2019
Single-molecule sequencing and chromatin conformation capture enable de novo reference assembly of the domestic goat genome
DM Bickhart, BD Rosen, S Koren, BL Sayre, AR Hastie, S Chan, J Lee, ...
Nature Genetics 49 (4), 643-650, 2017
Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity
JE Cleaver, ET Lam, I Revet
Nature Reviews Genetics 10 (11), 756-768, 2009
High-resolution comparative analysis of great ape genomes
ZN Kronenberg, IT Fiddes, D Gordon, S Murali, S Cantsilieris, ...
Science 360 (6393), eaar6343, 2018
Temporal dissection of tumorigenesis in primary cancers
S Durinck, C Ho, NJ Wang, W Liao, LR Jakkula, EA Collisson, J Pons, ...
Cancer Discovery 1 (2), 137-143, 2011
A hybrid approach for de novo human genome sequence assembly and phasing
Y Mostovoy, M Levy-Sakin, J Lam, ET Lam, AR Hastie, P Marks, J Lee, ...
Nature Methods, 2016
Rapid genome mapping in nanochannel arrays for highly complete and accurate de novo sequence assembly of the complex Aegilops tauschii genome
AR Hastie, L Dong, A Smith, J Finklestein, ET Lam, N Huo, H Cao, ...
PloS one 8 (2), 2013
Rapid detection of structural variation in a human genome using nanochannel-based genome mapping technology
H Cao, AR Hastie, D Cao, ET Lam, Y Sun, H Huang, X Liu, L Lin, ...
GigaScience 3 (1), 34, 2014
Assessing structural variation in a personal genome—towards a human reference diploid genome
AC English, WJ Salerno, OA Hampton, C Gonzaga-Jauregui, S Ambreth, ...
BMC Genomics 16 (1), 286, 2015
Genome-Wide Structural Variation Detection by Genome Mapping on Nanochannel Arrays
ACY Mak, YYY Lai, ET Lam, TP Kwok, AKY Leung, A Poon, Y Mostovoy, ...
Genetics 202 (1), 351-362, 2016
Sequencing of TNFAIP3 and association of variants with multiple autoimmune diseases
SL Musone, KE Taylor, J Nititham, C Chu, A Poon, W Liao, ET Lam, A Ma, ...
Genes and immunity 12 (3), 176-182, 2011
Genome maps across 26 human populations reveal population-specific patterns of structural variation
M Levy-Sakin, S Pastor, Y Mostovoy, L Li, AKY Leung, J McCaffrey, ...
Nature communications 10 (1), 1-14, 2019
Tools and pipelines for BioNano data: molecule assembly pipeline and FASTA super scaffolding tool
JM Shelton, MC Coleman, N Herndon, N Lu, ET Lam, T Anantharaman, ...
BMC Genomics 16 (1), 734, 2015
Role of Cyclin D1 as a Mediator of c-Met–and β-Catenin–Induced Hepatocarcinogenesis
MA Patil, SA Lee, E Macias, ET Lam, C Xu, KD Jones, C Ho, ...
Cancer research 69 (1), 253-261, 2009
Genome assembly and geospatial phylogenomics of the bed bug Cimex lectularius
JA Rosenfeld, D Reeves, MR Brugler, A Narechania, S Simon, R Durrett, ...
Nature communications 7, 2016
Mitochondrial DNA sequence variation and risk of pancreatic cancer
ET Lam, PM Bracci, EA Holly, C Chu, A Poon, E Wan, K White, PY Kwok, ...
Cancer research 72 (3), 686-695, 2012
Structural variation detection and analysis using Bionano optical mapping
S Chan, E Lam, M Saghbini, S Bocklandt, A Hastie, H Cao, E Holmlin, ...
Copy Number Variants, 193-203, 2018
Mitochondrial DNA sequence variation associated with dementia and cognitive function in the elderly
GJ Tranah, MA Nalls, SM Katzman, JS Yokoyama, ET Lam, Y Zhao, ...
Journal of Alzheimer's Disease 32 (2), 357-372, 2012
A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation
PM Martin, X Yang, N Robin, E Lam, JS Rabinowitz, CA Erdman, J Quinn, ...
Translational Psychiatry 3 (9), e301, 2013
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