Ami Levy-Moonshine
Current Protocols in Bioinformatics · 2013–2017
A researcher in the Science corpus: 3 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Whom Ami Levy-Moonshine trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Ami Levy-Moonshine's perspective
Ordered by how strongly the researchers Ami Levy-Moonshine trusts endorse each paper. Same corpus, a different order for every researcher.
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- Identification of common molecular subsequences.
- Transcriptome genetics using second generation sequencing in a Caucasian population (Nature)
- Understanding mechanisms underlying human gene expression variation with RNA sequencing (Nature)
- Biological Sequence Analysis: Probabilistic Models of Proteins and Nucleic Acids
- Transcriptome and genome sequencing uncovers functional variation in humans (Nature)
- dbSNP: the NCBI database of genetic variation
- An initial map of insertion and deletion (INDEL) variation in the human genome. (Genome Research)
- Mapping short DNA sequencing reads and calling variants using mapping quality scores. (Genome Research)
- Architecture of the human regulatory network derived from ENCODE data (Nature)
Their papers
- From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline (2013) — 6,636 citations
- Tools and best practices for data processing in allelic expression analysis (2015) — 359 citations
- Scaling accurate genetic variant discovery to tens of thousands of samples (2017) — 1,758 citations