Jouni Sirén
Genetics · 2018–2021
A researcher in the Science corpus: 2 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 24 citations into it
Whom Jouni Sirén trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from Jouni Sirén's perspective
Ordered by how strongly the researchers Jouni Sirén trusts endorse each paper. Same corpus, a different order for every researcher.
- A universal SNP and small-indel variant caller using deep neural networks
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
- An integrated map of structural variation in 2,504 human genomes (Nature)
- Reducing storage requirements for biological sequence comparison (Bioinform.)
- Transcriptome and genome sequencing uncovers functional variation in humans (Nature)
- A global reference for human genetic variation
- The design and construction of reference pangenome graphs with minigraph (Genome Biology)
- A structural variation reference for medical and population genetics (Nature)
- Biological Sequence Analysis: Probabilistic Models of Proteins and Nucleic Acids
- Minimap2: pairwise alignment for nucleotide sequences (Bioinform.)
Their papers
- Variation graph toolkit improves read mapping by representing genetic variation in the reference (2018) — 681 citations
- Pangenomics enables genotyping known structural variants in 5,202 diverse genomes (2021) — 309 citations