Adam Frankish
Molecular Biology · 2005–2024
A researcher in the Science corpus: 25 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 575 citations into it
Whom Adam Frankish trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Michael F. Lin
- W. James Kent
- Stephen F. Altschul
- J. Harrow
- Ana Kozomara
- Kim D. Pruitt
- R. Craig
- Avanti Shrikumar
- The UniProt Consortium
- Irwin Jungreis
Who trusts Adam Frankish overall
Papers from Adam Frankish's perspective
Ordered by how strongly the researchers Adam Frankish trusts endorse each paper. Same corpus, a different order for every researcher.
- Basic local alignment search tool.
- Human-mouse alignments with BLASTZ. (Genome Research)
- The Pfam protein families database
- GENCODE: producing a reference annotation for ENCODE (Genome Biology)
- Mapping and quantifying mammalian transcriptomes by RNA-Seq (Nature Methods)
- FAIRE (Formaldehyde-Assisted Isolation of Regulatory Elements) isolates active regulatory elements from human chromatin. (Genome Research)
- Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome (Nature Genetics)
- Transcriptional regulatory elements in the human genome. (Annual review of genomics and human genetics (Print))
- Antisense Transcription in the Mammalian Transcriptome (Science)
- The PeptideAtlas project (Nucleic Acids Res.)
Their papers
- GENCODE: producing a reference annotation for ENCODE (2006) — 695 citations
- GENCODE: The reference human genome annotation for The ENCODE Project (2012) — 4,487 citations
- The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes. (2009) — 586 citations
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) — 5,374 citations
- RNAcentral 2021: secondary structure integration, improved sequence search and new member databases (2020) — 337 citations
- A systematic survey of loss-of-function variants in human protein-coding genes (2012) — 1,227 citations
- The GENCODE pseudogene resource (2012) — 344 citations
- A joint NCBI and EMBL-EBI transcript set for clinical genomics and research (2022) — 465 citations
- Towards a complete map of the human long non-coding RNA transcriptome (2018) — 535 citations
- Ensembl 2022 (2021) — 465 citations
- GENCODE reference annotation for the human and mouse genomes (2018) — 2,759 citations
- Ensembl 2020 (2019) — 1,385 citations
- RNAcentral: a hub of information for non-coding RNA sequences (2018) — 303 citations
- Ensembl 2018 (2017) — 2,474 citations
- The DNA sequence of the human X chromosome (2005) — 1,099 citations
- Ensembl 2019 (2018) — 804 citations
- A User's Guide to the Encyclopedia of DNA Elements (ENCODE) (2011) — 1,042 citations
- Ensembl 2025 (2024) — 452 citations
- Ensembl 2024 (2023) — 566 citations
- Ensembl 2023 (2022) — 788 citations