Literature DB >> 15374870

MAP-O-MAT: internet-based linkage mapping.

X Kong1, T C Matise.   

Abstract

UNLABELLED: MAP-O-MAT is a web-based server for automated linkage mapping of human polymorphic DNA markers. MAP-O-MAT facilitates the verification of order and map distances for custom mapping sets using genotype data from the CEPH database, and from the Marshfield, SNP Consortium and Rutgers linkage maps (exclusive to the deCODE genotyping data). The CRI-MAP program is used for likelihood calculations and some mapping algorithms, and physical map positions are provided from the human genome assembly. AVAILABILITY: MAP-O-MAT is located at http://compgen.rutgers.edu/mapomat/ CONTACT: matise@biology.rutgers.edu.

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Year:  2004        PMID： 15374870     DOI： 10.1093/bioinformatics/bti024

Source DB:  PubMed          Journal:  Bioinformatics        ISSN： 1367-4803            Impact factor:   6.937


  15 in total

1.  Association of matrix metalloproteinase gene polymorphisms with refractive error in Amish and Ashkenazi families.

Authors:  Robert Wojciechowski; Joan E Bailey-Wilson; Dwight Stambolian
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-05-19       Impact factor: 4.799

2.  A combined linkage-physical map of the human genome.

Authors:  X Kong; K Murphy; T Raj; C He; P S White; T C Matise
Journal:  Am J Hum Genet       Date:  2004-10-14       Impact factor: 11.025

3.  A novel locus for autosomal recessive spastic ataxia on chromosome 17p.

Authors:  Naima Bouslam; Ahmed Bouhouche; Ali Benomar; Sylvain Hanein; Stephan Klebe; Hamid Azzedine; Silvia Di Giandomenico; Anne Boland-Augé; Filippo M Santorelli; Alexandra Durr; Alexis Brice; Mohamed Yahyaoui; Giovanni Stevanin
Journal:  Hum Genet       Date:  2007-02-02       Impact factor: 4.132

4.  Potentials and limits of pairwise kinship analysis using autosomal short tandem repeat loci.

Authors:  Michael Nothnagel; Jörg Schmidtke; Michael Krawczak
Journal:  Int J Legal Med       Date:  2010-02-10       Impact factor: 2.686

5.  A Novel Large Deletion Encompassing the Whole of the Galactose-1-Phosphate Uridyltransferase (GALT) Gene and Extending into the Adjacent Interleukin 11 Receptor Alpha (IL11RA) Gene Causes Classic Galactosemia Associated with Additional Phenotypic Abnormalities.

Authors:  Rena Papachristoforou; Petros P Petrou; Hilary Sawyer; Maggie Williams; Anthi Drousiotou
Journal:  JIMD Rep       Date:  2013-09-04

6.  LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

Authors:  Cyrus P Zabetian; Carolyn M Hutter; Dora Yearout; Alexis N Lopez; Stewart A Factor; Alida Griffith; Berta C Leis; Thomas D Bird; John G Nutt; Donald S Higgins; John W Roberts; Denise M Kay; Karen L Edwards; Ali Samii; Haydeh Payami
Journal:  Am J Hum Genet       Date:  2006-08-17       Impact factor: 11.025

7.  Translation initiator EIF4G1 mutations in familial Parkinson disease.

Authors:  Marie-Christine Chartier-Harlin; Justus C Dachsel; Carles Vilariño-Güell; Sarah J Lincoln; Frédéric Leprêtre; Mary M Hulihan; Jennifer Kachergus; Austen J Milnerwood; Lucia Tapia; Mee-Sook Song; Emilie Le Rhun; Eugénie Mutez; Lydie Larvor; Aurélie Duflot; Christel Vanbesien-Mailliot; Alexandre Kreisler; Owen A Ross; Kenya Nishioka; Alexandra I Soto-Ortolaza; Stephanie A Cobb; Heather L Melrose; Bahareh Behrouz; Brett H Keeling; Justin A Bacon; Emna Hentati; Lindsey Williams; Akiko Yanagiya; Nahum Sonenberg; Paul J Lockhart; Abba C Zubair; Ryan J Uitti; Jan O Aasly; Anna Krygowska-Wajs; Grzegorz Opala; Zbigniew K Wszolek; Roberta Frigerio; Demetrius M Maraganore; David Gosal; Tim Lynch; Michael Hutchinson; Anna Rita Bentivoglio; Enza Maria Valente; William C Nichols; Nathan Pankratz; Tatiana Foroud; Rachel A Gibson; Faycal Hentati; Dennis W Dickson; Alain Destée; Matthew J Farrer
Journal:  Am J Hum Genet       Date:  2011-09-09       Impact factor: 11.025

8.  Novel sequence variants in the TMIE gene in families with autosomal recessive nonsyndromic hearing impairment.

Authors:  Regie Lyn P Santos; Hatem El-Shanti; Shaheen Sikandar; Kwanghyuk Lee; Attya Bhatti; Kai Yan; Maria H Chahrour; Nathan McArthur; Thanh L Pham; Amjad Abdullah Mahasneh; Wasim Ahmad; Suzanne M Leal
Journal:  J Mol Med (Berl)       Date:  2005-12-31       Impact factor: 4.599

9.  A multilocus model of the genetic architecture of autoimmune thyroid disorder, with clinical implications.

Authors:  Veronica J Vieland; Yungui Huang; Christopher Bartlett; Terry F Davies; Yaron Tomer
Journal:  Am J Hum Genet       Date:  2008-05-15       Impact factor: 11.025

10.  A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type.

Authors:  M Naeem; M Wajid; K Lee; S M Leal; W Ahmad
Journal:  J Med Genet       Date:  2006-03       Impact factor: 6.318
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