This core facility provides automated fluorescent DNA sequencing services and automated oligonucleotide synthesis services to MRRC investigators. The core will service 30 investigators and 42 projected, a projected decrease over the past year. The facility is equipped with a substantial automated equipment and associated facilities to carry out the sequencing and oligonucleotide syntheses as well as excellent computer resources for analysis. Funding of the facility involves a credit allocation for approved MRRC investigators within the facility. Once their individual allocations have been exceeded they then pay on a recharge basis. Another facility provides MRRC investigators with 1) access to computer tools for pedigree and linkage analyses; 2) training on the use of these tools; 3) consultation on the appropriate use of these tools for genetic analysis of Mendelian and non-Mendelian phenotypes, and 4) generation of genotype data from DNAs provided by MRRC investigator. The third facility provides primary structural data on proteins and peptides to members of the MRRC. It generates peptide fragments, performs amino acid terminal sequence analysis, amino acid analyses, peptide synthesis, and certain types of molecular interaction studies. The facility is well equipped with several peptide synthesizers, protein sequencers and associated systems for peptide separation and analysis. It also provides consultation services to members of the MRRC. The Informatics Facility within the Genomics Core is intended to provide Center investigators expertise and assistance in bioinformatics and computational analysis. The core can provide Center investigators with access to both hardware and software for use in the analysis of nucleotide and protein sequence data, appropriate training in the proper use of these tools, provisions for the dissemination of data electronically to collaborators and the scientific community at large, and limited development of database solutions for the management of large amounts of sequence-based information.

Project Start
1998-09-11
Project End
1999-09-10
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
11
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Type
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Kho, Jordan; Tian, Xiaoyu; Wong, Wing-Tak et al. (2018) Argininosuccinate Lyase Deficiency Causes an Endothelial-Dependent Form of Hypertension. Am J Hum Genet 103:276-287
Eblimit, Aiden; Zaneveld, Smriti Agrawal; Liu, Wei et al. (2018) NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype. Exp Eye Res 173:32-43
Lanzieri, Tatiana M; Chung, Winnie; Leung, Jessica et al. (2018) Hearing Trajectory in Children with Congenital Cytomegalovirus Infection. Otolaryngol Head Neck Surg 158:736-744
Madan, Simran; Kron, Bettina; Jin, Zixue et al. (2018) Arginase overexpression in neurons and its effect on traumatic brain injury. Mol Genet Metab 125:112-117
De Maio, Antonia; Yalamanchili, Hari Krishna; Adamski, Carolyn J et al. (2018) RBM17 Interacts with U2SURP and CHERP to Regulate Expression and Splicing of RNA-Processing Proteins. Cell Rep 25:726-736.e7
Reeber, Stacey L; Arancillo, Marife; Sillitoe, Roy V (2018) Bergmann Glia are Patterned into Topographic Molecular Zones in the Developing and Adult Mouse Cerebellum. Cerebellum 17:392-403
Gillentine, Madelyn A; Lupo, Philip J; Stankiewicz, Pawel et al. (2018) An estimation of the prevalence of genomic disorders using chromosomal microarray data. J Hum Genet 63:795-801
Kariminejad, Ariana; Ajeawung, Norbert Fonya; Bozorgmehr, Bita et al. (2017) Kaufman oculo-cerebro-facial syndrome in a child with small and absent terminal phalanges and absent nails. J Hum Genet 62:465-471
Lanzieri, T M; Leung, J; Caviness, A C et al. (2017) Long-term outcomes of children with symptomatic congenital cytomegalovirus disease. J Perinatol 37:875-880
Zeng, Huan-Chang; Bae, Yangjin; Dawson, Brian C et al. (2017) MicroRNA miR-23a cluster promotes osteocyte differentiation by regulating TGF-? signalling in osteoblasts. Nat Commun 8:15000

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