T. Borodina
Molecular Biology · 2007–2015
A researcher in the Science corpus: 5 papers; trusts 1 researcher and is trusted by 16 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 50 citations into it; #3,637 of 17,773 by trust here, #1,272 by citations
Whom T. Borodina trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts T. Borodina overall
- Kimberly R. Kukurba
- Juliane C. Dohm
- Karl V. Voelkerding
- Davide Risso
- S. Deschamps
- Daniel R. Zerbino
- Desiree Tillo
- Kasper D. Hansen
Papers from T. Borodina's perspective
Ordered by how strongly the researchers T. Borodina trusts endorse each paper. Same corpus, a different order for every researcher.
- Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing (Nature Methods)
- An Eulerian path approach to DNA fragment assembly (Proceedings of the National Academy of Sciences of the United States of America)
- High-resolution profiling of histone methylations in the human genome. (Cell)
- Whole-genome re-sequencing. (Current Opinion in Genetics and Development)
- Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
- Initial sequencing and comparative analysis of the mouse genome (Nature)
- Assembling millions of short DNA sequences using SSAKE (Bioinform.)
- A whole-genome assembly of Drosophila. (Science)
- Genome sequencing in microfabricated high-density picolitre reactors (Nature)
- Whole-genome sequence assembly for mammalian genomes: Arachne 2. (Genome Research)
Their papers
- Substantial biases in ultra-short read data sets from high-throughput DNA sequencing (2008) — 1,181 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- SHARCGS, a fast and highly accurate short-read assembly algorithm for de novo genomic sequencing. (2007) — 318 citations
- Transcriptome analysis by strand-specific sequencing of complementary DNA (2009) — 950 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations