Your search for returned 25 results

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Resource

An integrative TAD catalog in lymphoblastoid cell lines discloses the functional impact of deletions and insertions in human genomes

  • First Published December 5, 2024
Method

Assessing and mitigating privacy risks of sparse, noisy genotypes by local alignment to haplotype databases

  • First Published December 14, 2023
Resource

Benchmarking small-variant genotyping in polyploids

  • First Published December 29, 2021
Research

Dynamic RNA–protein interactions underlie the zebrafish maternal-to-zygotic transition

  • First Published April 5, 2017
Research

Pangolin genomes and the evolution of mammalian scales and immunity

  • First Published August 10, 2016
Research

The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes

  • First Published March 11, 2013
Research

Chromatin state signatures associated with tissue-specific gene expression and enhancer activity in the embryonic limb

  • First Published March 15, 2012
Method

C. elegans by integrating conservation, secondary structure, and high-throughput sequencing and array data" > Prediction and characterization of noncoding RNAs in C. elegans by integrating conservation, secondary structure, and high-throughput sequencing and array data

  • First Published December 22, 2010
Research

Discovery of non-ETS gene fusions in human prostate cancer using next-generation RNA sequencing

  • First Published October 29, 2010
Resource

Dindel: Accurate indel calls from short-read data

  • First Published October 27, 2010
Resource

Stampy: A statistical algorithm for sensitive and fast mapping of Illumina sequence reads

  • First Published October 27, 2010
Research

Massive turnover of functional sequence in human and other mammalian genomes

  • First Published August 6, 2010
Method

Analysis of membrane proteins in metagenomics: Networks of correlated environmental features and protein families

  • First Published April 29, 2010
Method

Genome assembly quality: Assessment and improvement using the neutral indel model

  • First Published March 19, 2010
LETTER

Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history

  • First Published October 8, 2008
Methods

Uncertainty in homology inferences: Assessing and improving genomic sequence alignment

  • First Published December 11, 2007
LETTER

Statistical analysis of the genomic distribution and correlation of regulatory elements in the ENCODE regions

  • First Published June 13, 2007
LETTER

Structured RNAs in the ENCODE selected regions of the human genome

  • First Published June 13, 2007
Methods

Mapping of transcription factor binding regions in mammalian cells by ChIP: Comparison of array- and sequencing-based technologies

  • First Published June 13, 2007
ARTICLE

The DART classification of unannotated transcription within the ENCODE regions: Associating transcription with known and novel loci

  • First Published June 13, 2007
ARTICLE

Integrated analysis of experimental data sets reveals many novel promoters in 1% of the human genome

  • First Published June 13, 2007
PERSPECTIVE

What is a gene, post-ENCODE? History and updated definition

  • First Published June 13, 2007
ARTICLE

Functionality or transcriptional noise? Evidence for selection within long noncoding RNAs

  • First Published March 26, 2007
Methods

Assessing the performance of different high-density tiling microarray strategies for mapping transcribed regions of the human genome

  • First Published November 21, 2006
RESOURCE

Large-Scale Mutagenesis of the Yeast Genome Using a Tn7-Derived Multipurpose Transposon

  • First Published October 1, 2004
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