Rajini R Haraksingh

发表

Personal Omics Profiling Reveals Dynamic Molecular and Medical Phenotypes

Hugo Y. K. Lam, M. Gerstein, Donald Sharon, 2012, Cell.

Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway

Michael P. Snyder, A. Need, D. Goldstein, 2014, Genetics in Medicine.

Detecting and annotating genetic variations using the HugeSeq pipeline

Hugo Y. K. Lam, M. Gerstein, Michael P. Snyder, 2012, Nature Biotechnology.

Impacts of variation in the human genome on gene regulation.

M. Snyder, Rajini R Haraksingh, Michael P Snyder, 2013, Journal of molecular biology.

Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562.

Noah Spies, Dimitri Perrin, Wing H Wong, 2019, Genome research.

Consortium, G.P A map of human genome variation from population-scale sequencing. Nature 467, 1061-1073

Ken Chen, Joshua M. Korn, Afidalina Tumian, 2010 .

Whole-genome sequencing analysis of genomic copy number variation (CNV) using low-coverage and paired-end strategies is highly efficient and outperforms array-based CNV analysis

A. Urban, Rajini R Haraksingh, Bo Zhou, 2017, bioRxiv.

Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562

Hanlee P. Ji, John M. Bell, W. Wong, 2017, bioRxiv.

Child development and structural variation in the human genome.

M. Gerstein, Fabian Grubert, A. Abyzov, 2013, Child development.