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Human Genome Sequencing Center

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Trending Publications

The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities.
Genomic data in the All of Us Research Program.
Biallelic variation in the choline and ethanolamine transporter underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disorders.
Genetic sex validation for sample tracking in next-generation sequencing clinical testing.
The CARD8 inflammasome dictates HIV/SIV pathogenesis and disease progression.
Germline structural variation globally impacts the cancer transcriptome including disease-relevant genes.
Expanding the phenotype of PPP1R21-related neurodevelopmental disorder.
Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies.

Popular Publications

The house spider genome reveals an ancient whole-genome duplication during arachnid evolution.
Relationship between low-density lipoprotein subclasses and asymptomatic atherosclerosis in subjects from the Atherosclerosis Risk in Communities (ARIC) Study.
Convergent evolution of the genomes of marine mammals.
Genome-culture coevolution promotes rapid divergence of killer whale ecotypes.
Unique features of a global human ectoparasite identified through sequencing of the bed bug genome.
Genomic sequencing of key genes in mouse pancreatic cancer cells.
The sheep genome illuminates biology of the rumen and lipid metabolism.
The DNA sequence, annotation and analysis of human chromosome 3.

COVID-19 Research

Longitudinal host transcriptional responses to SARS-CoV-2 infection in adults with extremely high viral load.
Mental health trends among medical students.
Construction of a new chromosome-scale, long-read reference genome assembly for the Syrian hamster, Mesocricetus auratus.
Rescuing low frequency variants within intra-host viral populations directly from Oxford Nanopore sequencing data.
Read2Tree: scalable and accurate phylogenetic trees from raw reads.

Frequent Keywords

Humans 1,543

Female 739

Male 724

Animals 635

Mutation 337

Sequence Analysis, DNA 312

Polymorphism, Single Nucleotide 293

Phenotype 266

Middle Aged 246

Genomics 239

Genetic Predisposition to Disease 236

Mice 235

Adult 231

Molecular Sequence Data 230

Base Sequence 219

Genome, Human 211

Genetic Variation 208

Child 201

Pedigree 189

Genome-Wide Association Study 174

Exome 171

Adolescent 156

Child, Preschool 153

Genotype 153

High-Throughput Nucleotide Sequencing 149

Alleles 148

Aged 130

Genome 127

DNA Copy Number Variations 108

Chromosome Mapping 108

Phylogeny 103

Gene Frequency 99

Infant 98

Evolution, Molecular 97

Computational Biology 97

Young Adult 95

White People 95

Risk Factors 94

Genetic Association Studies 92

Amino Acid Sequence 90

Exome Sequencing 88

Gene Expression Profiling 85

Cohort Studies 83

Software 82

Polymerase Chain Reaction 80

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Baylor College of Medicine Human Genome Sequencing Center
Mail: One Baylor Plaza, MS: BCM226, Houston, TX 77030
Phone: 713-798-6539 | Fax: 713-798-5741
E-mail: questions@hgsc.bcm.edu

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Home
About Us
- People
- Funding
- News
- Contact Us
- Visiting HGSC
Careers
Projects
Publications
Software
- Atlas2
- ATLAS GapFill
- Atlas-Link
- Atlas Whole Genome Assembly Suite
- Bang
- bcm-ace-plots
- Cassandra
- CBT++
- CoCa
- DRAGEN
- ERIS
- ExCID Report
- Honey
- Jelly
- MegaDot
- Mercury
- Parliament2
- Princess
- SimPed
- Sniffles2
- SNP Tools
- SVCollector
- SVhound
- xAtlas
Resources