Pages that link to "Q65050486"
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The following pages link to NISC Comparative Sequencing Program (Q65050486):
Displaying 50 items.
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (Q21061203) (← links)
- Comparative analysis of the primate X-inactivation center region and reconstruction of the ancestral primate XIST locus (Q28744046) (← links)
- Variable molecular clocks in hominoids (Q28768556) (← links)
- Mutations in human homologue of chicken talpid3 gene (KIAA0586) cause a hybrid ciliopathy with overlapping features of Jeune and Joubert syndromes (Q29147550) (← links)
- First insight into the somatic mutation burden of neurofibromatosis type 2-associated grade I and grade II meningiomas: a case report comprehensive genomic study of two cranial meningiomas with vastly different clinical presentation (Q30274790) (← links)
- Massively-parallel sequencing of genes on a single chromosome: a comparison of solution hybrid selection and flow sorting (Q30455191) (← links)
- Using exome data to identify malignant hyperthermia susceptibility mutations (Q30689554) (← links)
- Evaluation of variant detection software for pooled next-generation sequence data (Q30983656) (← links)
- Replicate exome-sequencing in a multiple-generation family: improved interpretation of next-generation sequencing data (Q31027821) (← links)
- Uprobe 2008: an online resource for universal overgo hybridization-based probe retrieval and design (Q33339250) (← links)
- Comparative sequence analyses reveal sites of ancestral chromosomal fusions in the Indian muntjac genome (Q33379925) (← links)
- Homozygosity mapping and whole-exome sequencing to detect SLC45A2 and G6PC3 mutations in a single patient with oculocutaneous albinism and neutropenia (Q33395814) (← links)
- Dynamic evolution of V1R putative pheromone receptors between Mus musculus and Mus spretus (Q33407029) (← links)
- Distinct retroelement classes define evolutionary breakpoints demarcating sites of evolutionary novelty (Q33486715) (← links)
- Light whole genome sequence for SNP discovery across domestic cat breeds (Q33615383) (← links)
- Longitudinal shift in diabetic wound microbiota correlates with prolonged skin defense response (Q33644153) (← links)
- Gene-Specific Substitution Profiles Describe the Types and Frequencies of Amino Acid Changes during Antibody Somatic Hypermutation (Q33654599) (← links)
- Identification and characterization of multi-species conserved sequences (Q33683429) (← links)
- In silico and functional studies of the regulation of the glucocerebrosidase gene (Q33685329) (← links)
- Balancing selection maintains a form of ERAP2 that undergoes nonsense-mediated decay and affects antigen presentation (Q33728652) (← links)
- Staphylococcus epidermidis pan-genome sequence analysis reveals diversity of skin commensal and hospital infection-associated isolates (Q33741724) (← links)
- A rare myelin protein zero (MPZ) variant alters enhancer activity in vitro and in vivo (Q33778705) (← links)
- Lineage-specific evolution of the vertebrate Otopetrin gene family revealed by comparative genomic analyses (Q33801727) (← links)
- Comparative sequencing provides insights about the structure and conservation of marsupial and monotreme genomes (Q33852719) (← links)
- Integrative DNA, RNA, and protein evidence connects TREML4 to coronary artery calcification (Q33858743) (← links)
- Progressive proximal expansion of the primate X chromosome centromere (Q33906677) (← links)
- Conversion events in gene clusters (Q33974268) (← links)
- Genomic insights into Wnt signaling in an early diverging metazoan, the ctenophore Mnemiopsis leidyi (Q34024217) (← links)
- Adaptive evolution of foundation kinetochore proteins in primates (Q34029791) (← links)
- Low incidence of DNA sequence variation in human induced pluripotent stem cells generated by nonintegrating plasmid expression (Q34030950) (← links)
- A W-linked palindrome and gene conversion in New World sparrows and blackbirds (Q34070337) (← links)
- BAC-based sequencing of behaviorally-relevant genes in the prairie vole (Q34125043) (← links)
- Evolution of a bitter taste receptor gene cluster in a New World sparrow (Q34140291) (← links)
- Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing (Q34153640) (← links)
- Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy (Q34169437) (← links)
- Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegeneration (Q34238817) (← links)
- Biogeography and individuality shape function in the human skin metagenome (Q34290130) (← links)
- Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysis (Q34350807) (← links)
- Single-molecule sequencing to track plasmid diversity of hospital-associated carbapenemase-producing Enterobacteriaceae (Q34372097) (← links)
- Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants (Q34377776) (← links)
- Comparative exome sequencing of metastatic lesions provides insights into the mutational progression of melanoma (Q34420417) (← links)
- Global epigenomic analysis of primary human pancreatic islets provides insights into type 2 diabetes susceptibility loci (Q34518460) (← links)
- Novel somatic mutations in heterotrimeric G proteins in melanoma (Q34581746) (← links)
- A preliminary comparative analysis of primate segmental duplications shows elevated substitution rates and a great-ape expansion of intrachromosomal duplications (Q34591114) (← links)
- Enhanced potency of a broadly neutralizing HIV-1 antibody in vitro improves protection against lentiviral infection in vivo (Q34593860) (← links)
- Isolation, genomic structure and developmental expression of Fgf8 in the short-tailed fruit bat, Carollia perspicillata (Q34635339) (← links)
- Mutational analysis of the tyrosine kinome in serous and clear cell endometrial cancer uncovers rare somatic mutations in TNK2 and DDR1 (Q34650735) (← links)
- Mutational and functional analysis reveals ADAMTS18 metalloproteinase as a novel driver in melanoma (Q34682013) (← links)
- TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum (Q34764702) (← links)
- Analysis of primate genomic variation reveals a repeat-driven expansion of the human genome (Q34999165) (← links)