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Human Genome Sequencing Center
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Human Genome Sequencing Center - Faculty-General/Basic (Instructor)
Human Genome Sequencing Center - Informatics-Nex Gen (Associate Professor)
Postdoctoral Associate- Genomics
Postdoctoral Associate- Statistical Genetics Division: Human Genome Sequencing Center
Research Technician III
Projects
Clinical Lab
eMERGE
HeartCare
KidsCanSeq Study
RIGHT10K Study
TMC-CZI Project
Cancer Genomics
The Cancer Genome Atlas Project (TCGA)
Intracranial germ cell tumors
Pancreaticobiliary and duodenal tumors
Polycythemia vera
Human Genomics
Charcot-Marie-Tooth Project
CHARGE Consortium
eMERGE
Genomic Variation
Genomics and Space Medicine (Space Omics)
GREGoR
Human Genome Project
Ion Channel Project
SNP Discovery
Somatic Mosaicism Across Human Tissues (SMaHT)
Trans-Omics for Precision Medicine (TopMed)
Microbial Genomics
Microbial Projects
A. apis
A. castellani Neff
B. pumilus F036B
B. pumilus SAFR-032
D. crinitum OH494
D. discoideum AX4
E. coli DH10B
E. faecalis OG1
F. nucleatum ATCC10953
F. nucleatum ATCC23726
F. tularensis MI001730
F. tularensis OR96246
F. tularensis OSU18
F. tularensis RC503
Moraxella bovis Epp63
M. haemolytica PHL213
Paenibacillus larvae
P. stewartii
P. violaceum P6
R. typhi
S. aureus MRSA USA300
S. aureus MSSA
S. iniae
Texas Medical Center Genomic Center for Infectious Diseases (TMC GCID)
Microbiome Data Release Policy
Comparative
Non-human primates
Baboon
Black and white colobus
Chimpanzee
Drill
Gibbon
Marmoset
Mouse lemur
Orangutan
Owl monkey
Rhesus monkey
Sifaka lemur
Sooty mangabey
Other Mammals
Armadillo
Bovine
Hyrax
Kangaroo Rat
Megabat
Mouse
Peromyscus
Rat
Sheep
Wallaby
Y Chromosome
Marine Mammals
Dolphin
Killer whale
Reptiles
Adder
Arthropods
i5K Pilot
Asian long-horned beetle
Bark scorpion
Bed bug
Brown marmorated stink bug
Brown recluse spider
Bull-headed dung beetle
Caddisfly
Colorado potato beetle
Common house spider
Emerald ash borer
Eurytemora affinis
German cockroach
Glassy-Winged Sharpshooter
Hackberry petiole gall psyllid
Hrabe's jumping bristletail
Hyalella azteca
Mayfly
Mediterranean fruit fly
Milkweed bug
Parasitic wasp: T. pretiosum
Parasitic wasp: C. floridanum
Parasitic wood wasp: O. abietinus
Scarce Chaser
Sheep blowfly
Silvestri's Northern Forcepstail
Turnip sawfly
Velvet worm
Water strider
Western black widow spider
Western flower thrips
Aphid
Bees
Bumble Bee
Dwarf Honey Bee
Honey Bee
Drosophila
D. melanogaster
D. pseudoobscura
Library Construction
DGRP
DGRP Lines
modEncode
Black Fly
Butterfly
Centipede
Hessian Fly
Mite
Parasitic Wasp
Red flour beetle
Sand Fly
Tobacco Hornworm
Other Invertebrates
Acorn Worm
Cuttlefish
Sea Urchin
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
FTP Site
FTP Site Help
Conditions of use
HGSC Intranet
Glossary
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Popular Content
Mutations in PURA cause profound neonatal hypotonia, seizures, and encephalopathy in 5q31.3 microdeletion syndrome.
Fine structure of the human FMR1 gene.
Estimating population genetic parameters and comparing model goodness-of-fit using DNA sequences with error.
Whole Transcriptome Sequencing Analyses Reveal Molecular Markers of Blood Pressure Response to Thiazide Diuretics.
Biological and clinical significance of somatic mutations in Langerhans cell histiocytosis and related histiocytic neoplastic disorders.
Blood pressure signature genes and blood pressure response to thiazide diuretics: results from the PEAR and PEAR-2 studies.
Sequence analysis in reveals pervasiveness of X-Y arms races in mammalian lineages.
Analysis of HIV type 1 reverse transcriptase expression in a human cell line.
BEAUTY: an enhanced BLAST-based search tool that integrates multiple biological information resources into sequence similarity search results.
Comprehensive and Integrative Genomic Characterization of Hepatocellular Carcinoma.
Genomics. Genome project standards in a new era of sequencing.
Metabolomics and Incidence of Atrial Fibrillation in African Americans: The Atherosclerosis Risk in Communities (ARIC) Study.
PHENOTYPIC VARIABILITY OF RECESSIVE RDH12-ASSOCIATED RETINAL DYSTROPHY.
Finishing the euchromatic sequence of the human genome.
Effects of Gender-Specific Differences, Inflammatory Response, and Genetic Variation on the Associations Among Depressive Symptoms and the Risk of Major Adverse Coronary Events in Patients With Acute Coronary Syndrome.
Porin interaction with hexokinase and glycerol kinase: metabolic microcompartmentation at the outer mitochondrial membrane.
Genomes of the Hymenoptera.
Genetics: Decoding a national treasure.
The next generation of population-based spinal muscular atrophy carrier screening: comprehensive pan-ethnic SMN1 copy-number and sequence variant analysis by massively parallel sequencing.
Deletion screening at the hypoxanthine-guanine phosphoribosyltransferase locus in Chinese hamster cells using the polymerase chain reaction.
Apoptosis, autophagy, accelerated senescence and reactive oxygen in the response of human breast tumor cells to adriamycin.
[Theory of microcirculation. 1: Misinterpretations in Starling's hypothesis of microcirculation].
The genetic basis of DOORS syndrome: an exome-sequencing study.
A missense mutation in HK1 leads to autosomal dominant retinitis pigmentosa.
Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure.
The Consortium of Metabolomics Studies (COMETS): Metabolomics in 47 Prospective Cohort Studies.
The genome of th17 cell-inducing segmented filamentous bacteria reveals extensive auxotrophy and adaptations to the intestinal environment.
Comprehensive Genomic Characterization of Upper Tract Urothelial Carcinoma.
Identity and function of a large gene network underlying mutagenic repair of DNA breaks.
BRCA1/2 population screening: embracing the benefits.
High-throughput multiplex sequencing to discover copy number variants in Drosophila.
Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome.
The serotonin transporter genotype is associated with intermediate brain phenotypes that depend on the context of eliciting stressor.
Integrated genomic analyses of ovarian carcinoma.
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome.
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.
A server architecture for ambulatory patient record systems.
Fine mapping and characterization of candidate lung tumor resistance genes for the Par2 locus on mouse chromosome 18.
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.
Immunoglobulin locus associates with serum IgG levels and albuminuria.
Fat mass and obesity gene and cognitive decline: the Atherosclerosis Risk in Communities Study.
Identification of prognosis markers in pediatric high-risk acute lymphoblastic leukemia.
Is low-grade serous ovarian cancer part of the tumor spectrum of hereditary breast and ovarian cancer?
Targeting Thyroid Receptor b in Estrogen Receptor Negative Breast Cancer
Diabetes genes and prostate cancer in the Atherosclerosis Risk in Communities study.
Metabolomics and incident hypertension among blacks: the atherosclerosis risk in communities study.
De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea.
FBN1 contributing to familial congenital diaphragmatic hernia.
Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation.
Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.
Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line.
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium.
Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections.
Xia-Gibbs syndrome in adulthood: a case report with insight into the natural history of the condition.
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
Detection and characterization of the flagellar master operon in the four Shigella subgroups.
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum.
Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.
The relationship of JAK2(V617F) and acquired UPD at chromosome 9p in polycythemia vera.
Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology.
Taking DNA from the dead.
Identification of TP53 as an acute lymphocytic leukemia susceptibility gene through exome sequencing.
Comprehensive Molecular Diagnosis of a Large Chinese Leber Congenital Amaurosis Cohort.
Large-scale comparative sequence analysis of the human and murine Bruton's tyrosine kinase loci reveals conserved regulatory domains.
Transendothelial migration induces rapid expression on neutrophils of granule-release VLA6 used for tissue infiltration.
Characterization of the minimal replicator of Kaposi's sarcoma-associated herpesvirus latent origin.
GOSR2 Lys67Arg is associated with hypertension in whites.
Dicer-mediated upregulation of BCRP confers tamoxifen resistance in human breast cancer cells.
Loader Lite: a new software tool for the ABI PRISM 3700 DNA sequencer.
Involvement of SSRP1 in latent replication of Kaposi's sarcoma-associated herpesvirus.
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
New mutations in the RAB28 gene in 2 Spanish families with cone-rod dystrophy.
Challenges of Francisella classification exemplified by an atypical clinical isolate.
AluY insertion (IVS4-52ins316alu) in the glycerol kinase gene from an individual with benign glycerol kinase deficiency.
Exome sequencing identifies a homozygous C5orf42 variant in a Turkish kindred with oral-facial-digital syndrome type VI.
Deficiencies in vesicular transport mediated by TRAPPC4 are associated with severe syndromic intellectual disability.
Positional cloning of the major quantitative trait locus underlying lung tumor susceptibility in mice.
Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities.
The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance.
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI.
Squamous cell carcinoma of the oral tongue in young non-smokers is genomically similar to tumors in older smokers.
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.
Molecular and phenotypic variation in patients with severe Hunter syndrome.
Heritability of alveolar bone loss from periodontal disease in a baboon population: a pilot study.
A homozygous missense mutation in NEUROD1 is associated with nonsyndromic autosomal recessive retinitis pigmentosa.
Developing a tissue resource to characterize the genome of pancreatic cancer.
Complex genomic rearrangements at the PLP1 locus include triplication and quadruplication.
Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution.
Kaufman oculo-cerebro-facial syndrome in a child with small and absent terminal phalanges and absent nails.
Pretranscriptional regulation of Tgf-beta1 by PI polyamide prevents scarring and accelerates wound healing of the cornea after exposure to alkali.
Pentanucleotide repeat length polymorphism at the human CD4 locus.
Genome-enabled insights into the biology of thrips as crop pests.
REGγ is associated with multiple oncogenic pathways in human cancers.
The genomic organization of Isopeptidase T-3 (ISOT-3), a new member of the ubiquitin specific protease family (UBP).
UALCAN: A Portal for Facilitating Tumor Subgroup Gene Expression and Survival Analyses.
Mechanism of hedgehog signaling during Drosophila eye development.
Hsp90 modulates CAG repeat instability in human cells.
Treponema pallidum infection in the wild baboons of East Africa: distribution and genetic characterization of the strains responsible.
PipMaker--a web server for aligning two genomic DNA sequences.
Localization of multiple pleiotropic genes for lipoprotein metabolism in baboons.
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Home
About Us
People
Funding
News
Contact Us
Visiting HGSC
Careers
Human Genome Sequencing Center - Faculty-General/Basic (Instructor)
Human Genome Sequencing Center - Informatics-Nex Gen (Associate Professor)
Postdoctoral Associate- Genomics
Postdoctoral Associate- Statistical Genetics Division: Human Genome Sequencing Center
Research Technician III
Projects
Clinical Lab
eMERGE
HeartCare
KidsCanSeq Study
RIGHT10K Study
TMC-CZI Project
Cancer Genomics
The Cancer Genome Atlas Project (TCGA)
Intracranial germ cell tumors
Pancreaticobiliary and duodenal tumors
Polycythemia vera
Human Genomics
Charcot-Marie-Tooth Project
CHARGE Consortium
eMERGE
Genomic Variation
Genomics and Space Medicine (Space Omics)
GREGoR
Human Genome Project
Ion Channel Project
SNP Discovery
Somatic Mosaicism Across Human Tissues (SMaHT)
Trans-Omics for Precision Medicine (TopMed)
Microbial Genomics
Microbial Projects
A. apis
A. castellani Neff
B. pumilus F036B
B. pumilus SAFR-032
D. crinitum OH494
D. discoideum AX4
E. coli DH10B
E. faecalis OG1
F. nucleatum ATCC10953
F. nucleatum ATCC23726
F. tularensis MI001730
F. tularensis OR96246
F. tularensis OSU18
F. tularensis RC503
Moraxella bovis Epp63
M. haemolytica PHL213
Paenibacillus larvae
P. stewartii
P. violaceum P6
R. typhi
S. aureus MRSA USA300
S. aureus MSSA
S. iniae
Texas Medical Center Genomic Center for Infectious Diseases (TMC GCID)
Microbiome Data Release Policy
Comparative
Non-human primates
Baboon
Black and white colobus
Chimpanzee
Drill
Gibbon
Marmoset
Mouse lemur
Orangutan
Owl monkey
Rhesus monkey
Sifaka lemur
Sooty mangabey
Other Mammals
Armadillo
Bovine
Hyrax
Kangaroo Rat
Megabat
Mouse
Peromyscus
Rat
Sheep
Wallaby
Y Chromosome
Marine Mammals
Dolphin
Killer whale
Reptiles
Adder
Arthropods
i5K Pilot
Asian long-horned beetle
Bark scorpion
Bed bug
Brown marmorated stink bug
Brown recluse spider
Bull-headed dung beetle
Caddisfly
Colorado potato beetle
Common house spider
Emerald ash borer
Eurytemora affinis
German cockroach
Glassy-Winged Sharpshooter
Hackberry petiole gall psyllid
Hrabe's jumping bristletail
Hyalella azteca
Mayfly
Mediterranean fruit fly
Milkweed bug
Parasitic wasp: T. pretiosum
Parasitic wasp: C. floridanum
Parasitic wood wasp: O. abietinus
Scarce Chaser
Sheep blowfly
Silvestri's Northern Forcepstail
Turnip sawfly
Velvet worm
Water strider
Western black widow spider
Western flower thrips
Aphid
Bees
Bumble Bee
Dwarf Honey Bee
Honey Bee
Drosophila
D. melanogaster
D. pseudoobscura
Library Construction
DGRP
DGRP Lines
modEncode
Black Fly
Butterfly
Centipede
Hessian Fly
Mite
Parasitic Wasp
Red flour beetle
Sand Fly
Tobacco Hornworm
Other Invertebrates
Acorn Worm
Cuttlefish
Sea Urchin
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
FTP Site
FTP Site Help
Conditions of use
HGSC Intranet
Glossary