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QoRTs: a comprehensive toolset for quality control and data processing of RNA-Seq experiments

BMC bioinformatics, 2015-07, Vol.16 (1), p.224-224, Article 224

2015

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Systematic Evaluation of Sanger Validation of Next-Generation Sequencing Variants

Clinical chemistry (Baltimore, Md.), 2016-04, Vol.62 (4), p.647-654

2016

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Telomere-to-telomere assembly of a complete human X chromosome

Nature (London), 2020-09, Vol.585 (7823), p.79-84

2020

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Secondary Variants in Individuals Undergoing Exome Sequencing: Screening of 572 Individuals Identifies High-Penetrance Mutations in Cancer-Susceptibility Genes

American journal of human genetics, 2012-07, Vol.91 (1), p.97-108

2012

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Vaccine-Induced Antibodies that Neutralize Group 1 and Group 2 Influenza A Viruses

Cell, 2016-07, Vol.166 (3), p.609-623

2016

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Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease

Nature genetics, 2016-01, Vol.48 (1), p.67-73

2016

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Developmental pathway for potent V1V2-directed HIV-neutralizing antibodies

Nature (London), 2014-05, Vol.509 (7498), p.55-62

2014

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Low Incidence of DNA Sequence Variation in Human Induced Pluripotent Stem Cells Generated by Nonintegrating Plasmid Expression

Cell stem cell, 2012-03, Vol.10 (3), p.337-344

2012

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Single-molecule sequencing to track plasmid diversity of hospital-associated carbapenemase-producing Enterobacteriaceae

Science translational medicine, 2014-09, Vol.6 (254), p.254ra126

2014

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Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory disease

Proceedings of the National Academy of Sciences - PNAS, 2016-09, Vol.113 (36), p.10127-10132

2016

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Focused Evolution of HIV-1 Neutralizing Antibodies Revealed by Structures and Deep Sequencing

Science (American Association for the Advancement of Science), 2011-09, Vol.333 (6049), p.1593-1602

2011

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Measurement of the human allele frequency spectrum demonstrates greater genetic drift in East Asians than in Europeans

Nature genetics, 2007-10, Vol.39 (10), p.1251-1255

2007

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VarSifter: Visualizing and analyzing exome-scale sequence variation data on a desktop computer

Bioinformatics, 2012-02, Vol.28 (4), p.599-600

2012

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Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability

American journal of human genetics, 2017-02, Vol.100 (2), p.257-266

2017

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Mining the antibodyome for HIV-1-neutralizing antibodies with next-generation sequencing and phylogenetic pairing of heavy/light chains

Proceedings of the National Academy of Sciences - PNAS, 2013-04, Vol.110 (16), p.6470-6475

2013

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Developmental Pathway of the MPER-Directed HIV-1-Neutralizing Antibody 10E8

PloS one, 2016-06, Vol.11 (6), p.e0157409

2016

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Mutations in the Lysosomal Enzyme–Targeting Pathway and Persistent Stuttering

The New England journal of medicine, 2010-02, Vol.362 (8), p.677-685

2010

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De novo assembly of the goldfish ( Carassius auratus ) genome and the evolution of genes after whole-genome duplication

Science advances, 2019-06, Vol.5 (6), p.eaav0547-eaav0547

2019

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De novo identification of VRC01 class HIV-1–neutralizing antibodies by next-generation sequencing of B-cell transcripts

Proceedings of the National Academy of Sciences - PNAS, 2013-10, Vol.110 (43), p.17175-17175

2013

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Neurotranscriptomics: The Effects of Neonatal Stimulus Deprivation on the Rat Pineal Transcriptome

PloS one, 2015-09, Vol.10 (9), p.e0137548-e0137548

2015

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Somatic mutation profiles of clear cell endometrial tumors revealed by whole exome and targeted gene sequencing

Cancer, 2017-09, Vol.123 (17), p.3261-3268

2017

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QoRTs: a comprehensive toolset for quality control and data processing of RNA-Seq experiments

Systematic Evaluation of Sanger Validation of Next-Generation Sequencing Variants

Telomere-to-telomere assembly of a complete human X chromosome

Multidonor Analysis Reveals Structural Elements, Genetic Determinants, and Maturation Pathway for HIV-1 Neutralization by VRC01-Class Antibodies

Secondary Variants in Individuals Undergoing Exome Sequencing: Screening of 572 Individuals Identifies High-Penetrance Mutations in Cancer-Susceptibility Genes

Vaccine-Induced Antibodies that Neutralize Group 1 and Group 2 Influenza A Viruses

Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease

Developmental pathway for potent V1V2-directed HIV-neutralizing antibodies

Low Incidence of DNA Sequence Variation in Human Induced Pluripotent Stem Cells Generated by Nonintegrating Plasmid Expression

Co-evolution of a broadly neutralizing HIV-1 antibody and founder virus

Single-molecule sequencing to track plasmid diversity of hospital-associated carbapenemase-producing Enterobacteriaceae

Biallelic hypomorphic mutations in a linear deubiquitinase define otulipenia, an early-onset autoinflammatory disease

Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases

Maturation and Diversity of the VRC01-Antibody Lineage over 15 Years of Chronic HIV-1 Infection

Focused Evolution of HIV-1 Neutralizing Antibodies Revealed by Structures and Deep Sequencing

Measurement of the human allele frequency spectrum demonstrates greater genetic drift in East Asians than in Europeans

VarSifter: Visualizing and analyzing exome-scale sequence variation data on a desktop computer

Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability

Mining the antibodyome for HIV-1-neutralizing antibodies with next-generation sequencing and phylogenetic pairing of heavy/light chains

Developmental Pathway of the MPER-Directed HIV-1-Neutralizing Antibody 10E8

Mutations in the Lysosomal Enzyme–Targeting Pathway and Persistent Stuttering

De novo assembly of the goldfish ( Carassius auratus ) genome and the evolution of genes after whole-genome duplication

De novo identification of VRC01 class HIV-1–neutralizing antibodies by next-generation sequencing of B-cell transcripts

Neurotranscriptomics: The Effects of Neonatal Stimulus Deprivation on the Rat Pineal Transcriptome

Somatic mutation profiles of clear cell endometrial tumors revealed by whole exome and targeted gene sequencing

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