Nicholas A. Sinnott‐Armstrong

Directorate-General for Interpretation — Belgium

Biochemistry, Genetics and Molecular Biology · Life Sciences

18h-index11.9kcitations29works54.02yr avg
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Research Topics

Genomics and Chromatin Dynamics(9), Cancer Genomics and Diagnostics(7), Gene expression and cancer classification(6), RNA Research and Splicing(5), Genomics and Phylogenetic Studies(4)

Publications28 total

Long-range single-molecule mapping of chromatin accessibility in eukaryotes
Nature Methods·2020· 173 citedOpen Access
Corrigendum: Loss of LDAH associated with prostate cancer and hearing loss
Human Molecular Genetics·2019Open Access
Super-resolution chromatin tracing reveals domains and cooperative interactions in single cells
Science·2018· 1.0k citedOpen Access
Loss of <i>LDAH</i> associated with prostate cancer and hearing loss
Human Molecular Genetics·2018· 18 citedOpen Access
Diff-seq: A high throughput sequencing-based mismatch detection assay for DNA variant enrichment and discovery
Nucleic Acids Research·2018· 10 citedOpen Access
Pan-cancer screen for mutations in non-coding elements with conservation and cancer specificity reveals correlations with expression and survival
npj Genomic Medicine·2018· 84 citedOpen Access
Discovery and characterization of coding and non-coding driver mutations in more than 2,500 whole cancer genomes
2017· 47 citedOpen Access
Pan-cancer screen for mutations in non-coding elements with conservation and cancer specificity reveals correlations with expression and survival
2017· 6 citedOpen Access
Omni-ATAC-seq: Improved ATAC-seq protocol
Protocol Exchange·2017· 28 citedOpen Access
An improved ATAC-seq protocol reduces background and enables interrogation of frozen tissues
Nature Methods·2017· 2.6k citedOpen Access
An improved ATAC-seq protocol reduces background and enables interrogation of frozen tissues
2017· 28 citedOpen Access
Predicting gene expression in massively parallel reporter assays: A comparative study
Human Mutation·2017· 52 citedOpen Access
Convergence of dispersed regulatory mutations predicts driver genes in prostate cancer
2016· 13 citedOpen Access
Noncoding somatic and inherited single-nucleotide variants converge to promote ESR1 expression in breast cancer
Nature Genetics·2016· 100 cited
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
Nature Genetics·2016· 169 citedOpen Access
Integrative analysis of 111 reference human epigenomes
Nature·2015· 6.9k citedOpen Access
Integrative analysis of 111 reference human epigenomes
UWA Profiles and Research Repository (University of Western Australia)·2015Open Access
Cell-Based Metrics Improve the Detection of Gene-Gene Interactions Using Multifactor Dimensionality Reduction
Lecture notes in computer science·2013· 2 cited
GAMETES: a fast, direct algorithm for generating pure, strict, epistatic models with random architectures
BioData Mining·2012· 224 citedOpen Access
BioLite, a lightweight bioinformatics framework with automated tracking of diagnostics and provenance
2012· 14 cited
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Frequent Co-authors

Richard Sallari(9), Jason H. Moore(9), Manolis Kellis(8), Anshul Kundaje(7), M. Ryan Corces(4), Kathleen S. Montine(4), William J. Greenleaf(4), Alexandro E. Trevino(3), Emily G. Hamilton(3), Peyton Greenside(3), Sam Vesuna(3), Ansuman T. Satpathy(3), Adam J. Rubin(3), Beijing Wu(3), Arwa S. Kathiria(3), Maxwell R. Mumbach(3), Ava C. Carter(3), Maya Kasowski(3), Lisa A. Orloff(3), Viviana I. Risca(3)