Sara Ballouz, Alexander Dobin, Jesse A Gillis. Genome Biol 2019
Times Cited: 73
Times Cited: 73
Times Cited
Times Co-cited
Similarity
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Rachel M Sherman, Juliet Forman, Valentin Antonescu, Daniela Puiu, Michelle Daya, Nicholas Rafaels, Meher Preethi Boorgula, Sameer Chavan, Candelaria Vergara, Victor E Ortega,[...]. Nat Genet 2019
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Variation graph toolkit improves read mapping by representing genetic variation in the reference.
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Genome graphs and the evolution of genome inference.
Benedict Paten, Adam M Novak, Jordan M Eizenga, Erik Garrison. Genome Res 2017
Benedict Paten, Adam M Novak, Jordan M Eizenga, Erik Garrison. Genome Res 2017
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A global reference for human genetic variation.
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The Sequence Alignment/Map format and SAMtools.
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Heng Li, Bob Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gabor Marth, Goncalo Abecasis, Richard Durbin. Bioinformatics 2009
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FORGe: prioritizing variants for graph genomes.
Jacob Pritt, Nae-Chyun Chen, Ben Langmead. Genome Biol 2018
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One reference genome is not enough.
Xiaofei Yang, Wan-Ping Lee, Kai Ye, Charles Lee. Genome Biol 2019
Xiaofei Yang, Wan-Ping Lee, Kai Ye, Charles Lee. Genome Biol 2019
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Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype.
Daehwan Kim, Joseph M Paggi, Chanhee Park, Christopher Bennett, Steven L Salzberg. Nat Biotechnol 2019
Daehwan Kim, Joseph M Paggi, Chanhee Park, Christopher Bennett, Steven L Salzberg. Nat Biotechnol 2019
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The design and construction of reference pangenome graphs with minigraph.
Heng Li, Xiaowen Feng, Chong Chu. Genome Biol 2020
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Characterizing the Major Structural Variant Alleles of the Human Genome.
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Fast and accurate short read alignment with Burrows-Wheeler transform.
Heng Li, Richard Durbin. Bioinformatics 2009
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Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly.
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Heng Li. Bioinformatics 2011
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Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome.
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Graphtyper enables population-scale genotyping using pangenome graphs.
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Multi-platform discovery of haplotype-resolved structural variation in human genomes.
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Pan-Genome of Wild and Cultivated Soybeans.
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The Ensembl Variant Effect Predictor.
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Plant pan-genomes are the new reference.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.