Precise detection of rearrangement breakpoints in mammalian chromosomes
-
* Corresponding author: Claire Lemaitre clemaitr@biomserv.univ-lyon1.fr
1 Université de Lyon, F-69000, Lyon; Université Lyon 1; CNRS, UMR5558, Laboratoire de Biométrie et Biologie Evolutive, F-69622, Villeurbanne, France
2 Projet Helix, INRIA Rhône-Alpes, 655 avenue de l'Europe, 38330 Montbonnot Saint-Martin, France
BMC Bioinformatics 2008, 9:286 doi:10.1186/1471-2105-9-286
Published: 18 June 2008Additional files
Additional file 1:
Dataset of the breakpoints between human and mouse. The file contains the coordinates of the breakpoints obtained with the method described in the paper, with the human genome as reference, compared with the mouse genome. The breakpoints lie on the human genome (assembly version NCBI35). The file format is plain text, each line corresponds to one breakpoint, and there are three columns (chromosome, beginning and end positions of the breakpoint) separated by a space.
Format: TAB Size: 8KB Download file
Additional file 2:
Dataset of the breakpoints between human and dog. The file contains the coordinates of the breakpoints obtained with the method described in the paper, with the human genome as reference, compared with the dog genome. The breakpoints lie on the human genome (assembly version NCBI35). The file format is plain text, each line corresponds to one breakpoint, and there are three columns (chromosome, beginning and end positions of the breakpoint) separated by a space.
Format: TAB Size: 6KB Download file
