Pjotr Prins
Statistics and Probability · 2015–2022
A researcher in the Science corpus: 4 papers; trusts 2 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Statistics and Probability — 5 citations into it
Whom Pjotr Prins trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Pjotr Prins overall
Papers from Pjotr Prins's perspective
Ordered by how strongly the researchers Pjotr Prins trusts endorse each paper. Same corpus, a different order for every researcher.
- Rcpp: Seamless R and C++ Integration
- Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM
- A universal SNP and small-indel variant caller using deep neural networks
- Merqury: reference-free quality, completeness, and phasing assessment for genome assemblies (Genome Biology)
- Best Practices for Benchmarking Germline Small Variant Calls in Human Genomes (Nature Biotechnology)
- Multiple sequence alignment using partial order graphs
- Additional file 6
- Limitations of next-generation genome sequence assembly (Nature Methods)
- Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome (Nature Biotechnology)
- The design and construction of reference pangenome graphs with minigraph (Genome Biology)
Their papers
- Sambamba: fast processing of NGS alignment formats (2015) — 2,070 citations
- Tissue-specific mutation accumulation in human adult stem cells during life (2016) — 849 citations
- A draft human pangenome reference (2022) — 882 citations
- R/qtl2: Software for Mapping Quantitative Trait Loci with High-Dimensional Data and Multiparent Populations (2018) — 383 citations