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Human Genome Sequencing Center

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Trending Publications

Core planar cell polarity genes and in predisposition to congenital vertebral malformations.
Analysis and benchmarking of small and large genomic variants across tandem repeats.
Closing the gap: Solving complex medically relevant genes at scale.
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits.
The benefit of a complete reference genome for cancer structural variant analysis.
Unveiling microbial diversity: harnessing long-read sequencing technology.
Multilocus pathogenic variants contribute to intrafamilial clinical heterogeneity: a retrospective study of sibling pairs with neurodevelopmental disorders.
NODAL variants are associated with a continuum of laterality defects from simple D-transposition of the great arteries to heterotaxy.

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.
Unique features of a global human ectoparasite identified through sequencing of the bed bug genome.
Genome-culture coevolution promotes rapid divergence of killer whale ecotypes.
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 1,551

Female 741

Male 726

Animals 640

Mutation 338

Sequence Analysis, DNA 312

Polymorphism, Single Nucleotide 297

Phenotype 269

Middle Aged 246

Genomics 239

Genetic Predisposition to Disease 238

Mice 236

Adult 231

Molecular Sequence Data 230

Base Sequence 219

Genome, Human 214

Genetic Variation 210

Child 202

Pedigree 189

Genome-Wide Association Study 174

Exome 171

Adolescent 157

Genotype 155

Child, Preschool 154

High-Throughput Nucleotide Sequencing 151

Alleles 149

Aged 130

Genome 127

DNA Copy Number Variations 109

Chromosome Mapping 108

Phylogeny 103

Gene Frequency 100

Infant 99

Computational Biology 98

Evolution, Molecular 97

Young Adult 95

White People 95

Risk Factors 94

Genetic Association Studies 92

Amino Acid Sequence 90

Exome Sequencing 88

Gene Expression Profiling 86

Software 83

Cohort Studies 83

Black or African American 82

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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