Adam M. Phillippy
0000-0003-2983-8934
Publication & Citation Trends
Publications
0 total
SNP calling, haplotype phasing and allele-specific analysis with long RNA-seq reads
Cited by 0
Semantic Scholar
AniAnn's: alignment-free annotation of tandem repeat arrays using fast average nucleotide identity estimates
Cited by 0
Semantic Scholar
Fully Phased Telomere-to-Telomere Assemblies for Thoroughbred Horse and Donkey Haplotypes derived from a Mule Illuminate the Peculiar Evolution of Equid Centromeres
Cited by 0
Semantic Scholar
Biobank-scale genotyping of Robertsonian translocations reveals hidden structural variation on the human acrocentric chromosomes
Cited by 0
Semantic Scholar
Automatic Generation of Model Sequences for Complex Regions in Assembly Graphs
Cited by 0
Semantic Scholar
Using the linear references from the pangenome to discover missing autism variants
Cited by 2
Semantic Scholar
The complete genome of the KOLF2.1J reference iPSC line
Cited by 0
Semantic Scholar
Complex genetic variation in nearly complete human genomes
Cited by 28
Semantic Scholar
Research Topics
Genomics and Phylogenetic Studies
(175)
Chromosomal and Genetic Variations
(114)
RNA and protein synthesis mechanisms
(40)
Bacteriophages and microbial interactions
(34)
CRISPR and Genetic Engineering
(31)
Affiliations
Broad Institute
Human Genome Sciences (United States)
Stowers Institute for Medical Research
University of Maryland, Baltimore
National Institutes of Health