Your search for returned 34 results

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Method

Sequence-based correction of barcode bias in massively parallel reporter assays

  • First Published July 20, 2021
Method

Ancestry-agnostic estimation of DNA sample contamination from sequence reads

  • First Published January 24, 2020
Method

Human cardiac cis-regulatory elements, their cognate transcription factors, and regulatory DNA sequence variants

  • First Published August 23, 2018
Method

An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data

  • First Published April 16, 2015
Research

Divergent functions of hematopoietic transcription factors in lineage priming and differentiation during erythro-megakaryopoiesis

  • First Published October 15, 2014
Research

The influence of genomic context on mutation patterns in the human genome inferred from rare variants

  • First Published August 29, 2013
Method

Genotype calling and haplotyping in parent-offspring trios

  • First Published October 11, 2012
Method

Integration of ChIP-seq and machine learning reveals enhancers and a predictive regulatory sequence vocabulary in melanocytes

  • First Published September 27, 2012
Method

Discriminative prediction of mammalian enhancers from DNA sequence

  • First Published August 29, 2011
Resource

Low-coverage sequencing: Implications for design of complex trait association studies

  • First Published April 1, 2011
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