To display other sets of BACs on the current
build, use the
CViT-BACs page.
To query the location of nucleotide or amino
acid sequencess in the build, use the
CViT-Blast page.
BAC borders are shown on chromosomes. BAC and contig order has been determined
using evidence in this
order of preference: marker, then sequence overlap, then BAC end overlap (with at least 99%
identity over 90% of length, and only for low-copy BAC end matches), then
physical (FPC) map. In some cases, strong homology with sequenced regions of
Lotus japonicus has also been used. Contigs and supercontigs have also been ordered
where possible, using marker information. The MtChr0 "chromosome" consists of
unordered BACs and sequence contigs whose positions have not yet been determined.
BAC sequence contigs, scaffolds, and centromeric boundaries
BAC borders within sequence contigs and larger scaffolds (supercontigs) are shown as follows:
Light gray indicates BAC borders that are inside sequence contigs;
black indicates "hard gaps" of unknown size.
Approximate centromeric boundaries are flanked by red lines. Candidate flanking BACs:
AC151619 AC135959
AC124609 AC146756
AC147201 AC147407
AC145289 AC119416
AC135848 AC135101/AC140031
AC135464 AC138199
AC121242 AC124215
AC147006 AC146723
BACs By Sequencing Center
Shows BACs sequenced by center:
University of Oklahoma
TIGR
Genoscope
Sanger Institute
"Other"
Mapped BACs
BAC borders are shown on chromosomes. Light gray indicates BAC borders that are
inside contigs; black BACs are on edges of contigs. The lines between BACs indicate
gaps of unknown length.