Eric Banks

发表

Analyzing and Interrogating Biological Networks (Abstract)

Mona Singh, Bernard Chazelle, Eric Banks, 2009, BICoB.

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

Yeting Zhang, Heng Li, Eric Banks, 2018 .

Efficiency and Power as a Function of Sequence Coverage, SNP Array Density, and Imputation

Joshua M. Korn, Pierre Fontanillas, Eric Banks, 2012, PLoS Comput. Biol..

The variant call format and VCFtools

Gonçalo R. Abecasis, Richard Durbin, Stephen T. Sherry, 2011, Bioinform..

A structural variation reference for medical and population genetics

Tariq Ahmad, Patrick F. Sullivan, Mark I. McCarthy, 2020, Nature.

ContEst: estimating cross-contamination of human samples in next-generation sequencing data

Kristian Cibulskis, Eric Banks, Gad Getz, 2011, Bioinform..

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

Yeting Zhang, Heng Li, Eric Banks, 2018, Nature Communications.

Lean and deep models for more accurate filtering of SNP and INDEL variant calls

Sam Friedman, Eric Banks, Yossi Farjoun, 2019, Bioinform..

Tools and best practices for allelic expression analysis

Eric Banks, Stephane E. Castel, Pejman Mohammadi, 2015, bioRxiv.

Organization of Physical Interactomes as Uncovered by Network Schemas

Mona Singh, Bernard Chazelle, Eric Banks, 2008, PLoS Comput. Biol..

Abstract 5108: Somatic small variant and copy number alteration calling with the Genome Analysis Toolkit

Kristian Cibulskis, David Benjamin, Eric Banks, 2019 .

A framework for the detection of de novo mutations in family-based sequencing data

Eric Banks, Menachem Fromer, Benjamin M Neale, 2016, European Journal of Human Genetics.

A polygenic burden of rare disruptive mutations in schizophrenia

Eric S. Lander, Patrick F. Sullivan, Jyoti S. Choudhary, 2014, Nature.

Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls

Kathryn Roeder, Stephan Ripke, Shannon Gross, 2013, PLoS genetics.

Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction

Eric Banks, Sekar Kathiresan, Leif Groop, 2011, Nature Genetics.

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Tariq Ahmad, Patrick F. Sullivan, Andres Metspalu, 2020, Nature Communications.

MacArthur Protein-Coding Genes A Systematic Survey of Loss-of-Function Variants in Human

Klaudia Walter, Joseph K. Pickrell, Jennifer Harrow, 2012 .

Exome Aggregation Consortium

Adam Kiezun, Sergio Islas-Andrade, Pierre Fontanillas, 2016 .

Mapping and characterization of structural variation in 17,795 human genomes

Eric S. Lander, Haley J. Abel, Yeting Zhang, 2020, Nature.

An open resource of structural variation for medical and population genetics

Grace Tiao, Daniel G. MacArthur, Ryan L. Collins, 2019 .

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 .

Tools and best practices for data processing in allelic expression analysis

Eric Banks, Stephane E. Castel, Pejman Mohammadi, 2015, Genome Biology.

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Taesung Park, Christian Gieger, Tien Yin Wong, 2017, Scientific Data.

A TALEN genome-editing system for generating human stem cell-based disease models.

Kevin Kim, Eric Banks, Feng Zhang, 2013, Cell stem cell.

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Tariq Ahmad, Patrick F. Sullivan, Andres Metspalu, 2019, bioRxiv.