Ernest T Lam


Ontology type: schema:Person     


Person Info

NAME

Ernest T

SURNAME

Lam

Publications in SciGraph latest 50 shown

  • 2018-07-24 Structural Variation Detection and Analysis Using Bionano Optical Mapping in COPY NUMBER VARIANTS
  • 2017-12 OMSV enables accurate and comprehensive identification of large structural variations from nanochannel-based single-molecule optical maps in GENOME BIOLOGY
  • 2017-04 Single-molecule sequencing and chromatin conformation capture enable de novo reference assembly of the domestic goat genome in NATURE GENETICS
  • 2016-07 A hybrid approach for de novo human genome sequence assembly and phasing in NATURE METHODS
  • 2016 Towards a More Accurate Error Model for BioNano Optical Maps in BIOINFORMATICS RESEARCH AND APPLICATIONS
  • 2015-12 Tools and pipelines for BioNano data: molecule assembly pipeline and FASTA super scaffolding tool in BMC GENOMICS
  • 2015-12 Assessing structural variation in a personal genome—towards a human reference diploid genome in BMC GENOMICS
  • 2014-12 Rapid detection of structural variation in a human genome using nanochannel-based genome mapping technology in GIGASCIENCE
  • 2014-12 Erratum to: Application of next generation sequencing to CEPH cell lines to discover variants associated with FDA approved chemotherapeutics in BMC RESEARCH NOTES
  • 2013-09 A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation in TRANSLATIONAL PSYCHIATRY
  • 2012-08 Genome mapping on nanochannel arrays for structural variation analysis and sequence assembly in NATURE BIOTECHNOLOGY
  • 2012-05 Pharmacogene regulatory elements: from discovery to applications in GENOME MEDICINE
  • 2011-12 Timing chromosomal abnormalities using mutation data in GENOME BIOLOGY
  • 2011-12 Timing chromosomal abnormalities using mutation data in GENOME BIOLOGY
  • 2011-12 Association analysis identifies ZNF750 regulatory variants in psoriasis in BMC MEDICAL GENETICS
  • 2011-04 Sequencing of TNFAIP3 and association of variants with multiple autoimmune diseases in GENES & IMMUNITY
  • 2009-11 Disorders of nucleotide excision repair: the genetic and molecular basis of heterogeneity in NATURE REVIEWS GENETICS
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