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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
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Atlas2
ATLAS GapFill
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Atlas Whole Genome Assembly Suite
Bang
bcm-ace-plots
Cassandra
CBT++
CoCa
DRAGEN
ERIS
ExCID Report
Honey
Jelly
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Parliament2
Princess
SimPed
Sniffles2
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Popular Content
Notch activation as a driver of osteogenic sarcoma.
Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.
A proposed architecture for ambulatory systems development.
A physical map of the human genome.
Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome.
The use of primers from highly conserved pol regions to identify uncharacterized retroviruses by the polymerase chain reaction.
PNPLA3 polymorphisms and liver aminotransferase levels in a Mexican American population.
Dynamic analyses of alternative polyadenylation from RNA-seq reveal a 3'-UTR landscape across seven tumour types.
Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion.
Pan-Cancer Molecular Classes Transcending Tumor Lineage Across 32 Cancer Types, Multiple Data Platforms, and over 10,000 Cases.
Are feeding preferences and insecticide resistance associated with the size of detoxifying enzyme families in insect herbivores?
Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies.
Editorial overview: Insect genomics: Arthropod genomic resources for the 21st century: It only counts if it's in the database!
Integrative genomic characterization of oral squamous cell carcinoma identifies frequent somatic drivers.
ABCF1 extrinsically regulates retinal pigment epithelial cell phagocytosis.
Elimination of residual natural nucleotides from 3'-O-modified-dNTP syntheses by enzymatic mop-up.
A transposon-like element in the deletion-prone region of the dystrophin gene.
Genetic influences on behavioral inhibition and anxiety in juvenile rhesus macaques.
A human dimorphism resulting from loss of an Alu.
Cerebral visual impairment and intellectual disability caused by PGAP1 variants.
Rapid identification of heterozygous mutations in Drosophila melanogaster using genomic capture sequencing.
The 1000 Genomes Project: data management and community access.
Genomics Research to Elucidate the Genetics of Rare diseases (GREGoR)
Parent of origin, mosaicism, and recurrence risk: probabilistic modeling explains the broken symmetry of transmission genetics.
Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels.
Accurate determination of DNA in agarose gels using the novel algorithm GelScann(1.0).
Apparent underdiagnosis of Cerebrotendinous Xanthomatosis revealed by analysis of ~60,000 human exomes.
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
Fine mapping of chromosome 6q23-25 region in familial lung cancer families reveals RGS17 as a likely candidate gene.
ANGPTL3 Deficiency and Protection Against Coronary Artery Disease.
The clinical applications of The Cancer Genome Atlas project for bladder cancer.
Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosa.
Recurrent duplication-driven transposition of DNA during hominoid evolution.
A genetic association study of activated partial thromboplastin time in European Americans and African Americans: the ARIC Study.
Mutations in human IFT140 cause non-syndromic retinal degeneration.
Pas1c1 is a candidate for the mouse pulmonary adenoma susceptibility 1 locus.
Comprehensive analysis of patients with Stargardt macular dystrophy reveals new genotype-phenotype correlations and unexpected diagnostic revisions.
Method for 96-well M13 DNA template preparations for large-scale sequencing.
Divergent Levels of Marker Chromosomes in an hiPSC-Based Model of Psychosis.
Positive selection of a pre-expansion CAG repeat of the human SCA2 gene.
POU6f1 Mediates Neuropeptide-Dependent Plasticity in the Adult Brain.
Variability of dopamine D4 receptor (DRD4) gene sequence within and among nonhuman primate species.
Piercing the dark matter: bioinformatics of long-range sequencing and mapping.
Microarray analysis of somatostatin receptor 5-regulated gene expression profiles in murine pancreas.
Single nucleotide polymorphism in RECQL and survival in resectable pancreatic adenocarcinoma.
Genomic Characterization of Sinonasal Undifferentiated Carcinoma
Generation and annotation of the DNA sequences of human chromosomes 2 and 4.
ADD1 460W allele associated with cardiovascular disease in hypertensive individuals.
The alpha-amino-3-hydroxyl-5-methyl-4-isoxazolepropionate receptor trafficking regulator "stargazin" is related to the claudin family of proteins by Its ability to mediate cell-cell adhesion.
Genomic and SNP analyses demonstrate a distant separation of the hospital and community-associated clades of Enterococcus faecium.
Mutations in ASH1L confer susceptibility to Tourette syndrome.
Widespread lateral gene transfer from intracellular bacteria to multicellular eukaryotes.
Whole-exome sequencing of polycythemia vera revealed novel driver genes and somatic mutation shared by T cells and granulocytes.
WormBase: a multi-species resource for nematode biology and genomics.
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
Comparative genomics of Gardnerella vaginalis strains reveals substantial differences in metabolic and virulence potential.
Cloning and functional expression of the hNPY Y5 receptor in human endometrial cancer (HEC-1B) cells.
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease.
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.
Improved ligation-anchored PCR strategy for identification of 5' ends of transcripts.
FOXO1 is required for binding of PR on IRF4, novel transcriptional regulator of endometrial stromal decidualization.
Identification of Polycystic Kidney Disease 1 Like 1 Gene Variants in Children With Biliary Atresia Splenic Malformation Syndrome.
The DNA sequence of human chromosome 7.
Epigenomic profiling of young and aged HSCs reveals concerted changes during aging that reinforce self-renewal.
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia.
Long-range massively parallel mate pair sequencing detects distinct mutations and similar patterns of structural mutability in two breast cancer cell lines.
COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis.
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.
Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci.
Next-generation sequencing and novel variant determination in a cohort of 92 familial exudative vitreoretinopathy patients.
Identification of genetic susceptibility to childhood cancer through analysis of genes in parallel.
No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects.
Genomic encyclopedia of bacteria and archaea: sequencing a myriad of type strains.
PCR test for cystic fibrosis deletion.
Scale-invariant structure of strongly conserved sequence in genomic intersections and alignments.
Elevated expression of DNA polymerase II increases spontaneous mutagenesis in Escherichia coli.
Secondary findings and carrier test frequencies in a large multiethnic sample.
Pooled genomic indexing of rhesus macaque.
Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3.
SYT1-associated neurodevelopmental disorder: a case series.
CRISPR-engineered mosaicism rapidly reveals that loss of Kcnj13 function in mice mimics human disease phenotypes.
Molecular findings among patients referred for clinical whole-exome sequencing.
Genotypic confirmation from the original dried blood specimens in a neonatal hemoglobinopathy screening program.
Whole exome sequencing confirms the clinical diagnosis of Marfan syndrome combined with X-linked hypophosphatemia.
Unusual sequence characteristics of human chromosome 19 are conserved across 11 nonhuman primates.
Mechanisms underlying structural variant formation in genomic disorders.
Improved annotation of the insect vector of citrus greening disease: biocuration by a diverse genomics community.
Combination of whole exome sequencing and animal modeling identifies TMPRSS9 as a candidate gene for autism spectrum disorder.
The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer.
Comprehensive genomic characterization defines human glioblastoma genes and core pathways.
Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations.
Genomes of the Hymenoptera
Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans.
An Organismal CNV Mutator Phenotype Restricted to Early Human Development.
Phenotypic expansion of TBX4 mutations to include acinar dysplasia of the lungs.
Long HIV-1 incubation periods and dynamics of transmission within a family.
NR2F1 mutations cause optic atrophy with intellectual disability.
Large-scale sequencing in human chromosome 12p13: experimental and computational gene structure determination.
Gastrointestinal microbiome signatures of pediatric patients with irritable bowel syndrome.
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Home
About Us
People
Funding
News
Contact Us
Visiting HGSC
Careers
Postdoctoral Associate- Genomics
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