Your search for returned 48 results

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Method

Deep sequencing of short capped RNAs reveals novel families of noncoding RNAs

  • First Published August 12, 2022
Method

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

  • First Published July 20, 2021
Research

Comparative transcriptomics of primary cells in vertebrates

  • First Published July 27, 2020
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
Research

The frequent evolutionary birth and death of functional promoters in mouse and human

  • First Published July 30, 2015
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
Method

Comparison of CAGE and RNA-seq transcriptome profiling using clonally amplified and single-molecule next-generation sequencing

  • First Published March 27, 2014
Research

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

  • First Published August 29, 2013
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