Alexej Abyzov
Nature · 2011–2015
A researcher in the Science corpus: 10 papers; trusts 2 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Whom Alexej Abyzov trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Alexej Abyzov overall
Papers from Alexej Abyzov's perspective
Ordered by how strongly the researchers Alexej Abyzov trusts endorse each paper. Same corpus, a different order for every researcher.
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
- The Human Gene Mutation Database: 2008 update
- Genome-Wide Mapping of in Vivo Protein-DNA Interactions (Science)
- FAIRE (Formaldehyde-Assisted Isolation of Regulatory Elements) isolates active regulatory elements from human chromatin. (Genome Research)
- Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing (Nature Methods)
- Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome (Nature Genetics)
- Control of developmental regulators by Polycomb in human embryonic stem cells. (Cell)
- Transcriptional regulatory elements in the human genome. (Annual review of genomics and human genetics (Print))
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
Their papers
- Architecture of the human regulatory network derived from ENCODE data (2012) — 1,495 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics (2013) — 370 citations
- AlleleSeq: analysis of allele-specific expression and binding in a network framework (2011) — 352 citations
- A User's Guide to the Encyclopedia of DNA Elements (ENCODE) (2011) — 1,042 citations
- FOXG1-dependent dysregulation of GABA/glutamate neuron differentiation in autism spectrum disorders (2015) — 1,017 citations
- An integrated map of structural variation in 2,504 human genomes (2015) — 2,247 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
- Mapping copy number variation by population scale genome sequencing (2011) — 1,130 citations
- CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. (2011) — 1,610 citations