Literature DB >> 8808581

SAM: a system for iteratively building marker maps.

C Soderlund1, I Dunham.   

Abstract

SAM (system for assembling markers) is a system which supports man-machine problem solving for iteratively ordering a set of markers. SAM aids the user in partially ordering a set of markers based on incomplete and uncertain data. As data is added and modified, SAM aids the user in updating the previously assembled maps. The input is a file of clones and for each clone, a list of the markers contained within it. The objective is to order the set of markers such that the markers contained in each clone are consecutive. The user directs the map building by selecting functions to assemble a region of markers, order the clones to fit the order of the markers and position new markers within an ordered set of markers. The user can edit the input data, edit the assembled map and add clones to the map based on their marker content. The results are displayed graphically and can be saved in a solution file. Based on the partial map, the user designs new experiments or edits the existing data to fill gaps and resolve ambiguities. When a previously assembled map is loaded into SAM, it is automatically updated with the new or altered data. SAM treats all markers as points, but has special features for multiple copy and long markers so that they can be used in the map building process. This system has supported the building of a YAC map of human chromosome 22 at the Sanger Centre, where use of Alu-PCR product markers is a major component in determining clone overlap and where we have an on-going effort to accumulate data from various sources. SAM is also being used at various other laboratories.

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Year:  1995        PMID: 8808581     DOI: 10.1093/bioinformatics/11.6.645

Source DB:  PubMed          Journal:  Comput Appl Biosci        ISSN: 0266-7061


  8 in total

1.  High-resolution landmark framework for the sequence-ready mapping of Xq23-q26.1.

Authors:  H E Steingruber; A Dunham; A J Coffey; S M Clegg; G R Howell; G L Maslen; C E Scott; R Gwilliam; P J Hunt; E C Sotheran; E J Huckle; S E Hunt; P Dhami; C Soderlund; M A Leversha; D R Bentley; M T Ross
Journal:  Genome Res       Date:  1999-08       Impact factor: 9.043

2.  A 7.5 Mb sequence-ready PAC contig and gene expression map of human chromosome 11p13-p14.1.

Authors:  B Gawin; A Niederführ; N Schumacher; H Hummerich; P F Little; M Gessler
Journal:  Genome Res       Date:  1999-11       Impact factor: 9.043

3.  ODS2: a multiplatform software application for creating integrated physical and genetic maps.

Authors:  D Hall; S M Bhandarkar; J Wang
Journal:  Genetics       Date:  2001-03       Impact factor: 4.562

4.  Anchoring of a large set of markers onto a BAC library for the development of a draft physical map of the grapevine genome.

Authors:  Didier Lamoureux; Anne Bernole; Isabelle Le Clainche; Sarah Tual; Vincent Thareau; Sophie Paillard; Fabrice Legeai; Carole Dossat; Patrick Wincker; Marilyn Oswald; Didier Merdinoglu; Céline Vignault; Serge Delrot; Michel Caboche; Boulos Chalhoub; Anne-Françoise Adam-Blondon
Journal:  Theor Appl Genet       Date:  2006-05-18       Impact factor: 5.699

5.  HOSEpipe--a WWW-hosted data management and analysis system for STS content mapping projects.

Authors:  M A Strivens; P Middlehurst; S D Brown; P Denny
Journal:  Mamm Genome       Date:  1997-07       Impact factor: 2.957

6.  Toward integration of comparative genetic, physical, diversity, and cytomolecular maps for grasses and grains, using the sorghum genome as a foundation.

Authors:  X Draye; Y R Lin; X Y Qian; J E Bowers; G B Burow; P L Morrell; D G Peterson; G G Presting; S X Ren; R A Wing; A H Paterson
Journal:  Plant Physiol       Date:  2001-03       Impact factor: 8.340

7.  Contigs built with fingerprints, markers, and FPC V4.7.

Authors:  C Soderlund; S Humphray; A Dunham; L French
Journal:  Genome Res       Date:  2000-11       Impact factor: 9.043

8.  Computational comparison of human genomic sequence assemblies for a region of chromosome 4.

Authors:  Colin A M Semple; Stewart W Morris; David J Porteous; Kathryn L Evans
Journal:  Genome Res       Date:  2002-03       Impact factor: 9.043

  8 in total

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