Gabor T. Marth
Molecular Biology · 2008–2017
A researcher in the Science corpus: 12 papers; trusts 19 researchers and is trusted by 23 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 144 citations into it; #1,562 of 17,773 by trust here, #261 by citations
- Genetics — 120 citations into it; #1,877 of 6,854 by trust here, #50 by citations
- Artificial Intelligence — 14 citations into it; #17,354 of 35,345 by trust here, #1,309 by citations
- Ecology — 7 citations into it
- Computational Biology & Bioinformatics — 6 citations into it
Whom Gabor T. Marth trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Heng Li
- Richard Maclin
- Bryan N. Howie
- Yun Li
- Temple F. Smith
- James Clarke
- Andrzej Wozniak
- William R. Pearson
- Mark A. DePristo
- Jonathan Marchini
Who trusts Gabor T. Marth overall
- Nicolas C. Rochette
- Heng Li
- Daniel C. Koboldt
- Todd J. Treangen
- Julian Catchen
- Raquel Dias
- Ryan Poplin
- Arang Rhie
- Sergey Koren
- P. Park
Papers from Gabor T. Marth's perspective
Ordered by how strongly the researchers Gabor T. Marth 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.
- The Human Gene Mutation Database: 2008 update
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- The Diploid Genome Sequence of an Individual Human (PLoS Biology)
- MaCH: Using Sequence and Genotype Data to Estimate Haplotypes and Unobserved Genotypes (Genetic Epidemiology)
- A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data (Bioinform.)
- The human genome browser at UCSC.
- SOAP: short oligonucleotide alignment program (Bioinform.)
- Next-generation DNA sequencing methods. (Annual review of genomics and human genetics (Print))
Their papers
- The Sequence Alignment/Map format and SAMtools (2009) — 56,954 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- Multi-platform discovery of haplotype-resolved structural variation in human genomes (2017) — 796 citations
- Haplotype-based variant detection from short-read sequencing (2012) — 4,999 citations
- SSW Library: An SIMD Smith-Waterman C/C++ Library for Use in Genomic Applications (2012) — 246 citations
- Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics (2013) — 370 citations
- Whole-genome sequencing and variant discovery in C. elegans (2008) — 454 citations
- MOSAIK: A Hash-Based Algorithm for Accurate Next-Generation Sequencing Short-Read Mapping (2013) — 295 citations
- BamTools: a C++ API and toolkit for analyzing and managing BAM files (2011) — 969 citations
- An integrated map of structural variation in 2,504 human genomes (2015) — 2,247 citations
- SpeedSeq: Ultra-fast personal genome analysis and interpretation (2014) — 544 citations
- Demographic history and rare allele sharing among human populations (2011) — 660 citations