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- CViT-blast utility -
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Blast a fasta-format sequence or set of sequences against the current Medicago
truncatula psuedochromosome build. The output page will show two views of the
blast hits: a compressed image, an expanded image that also shows BAC borders, and
a table describing the hits. See the FAQs for more information.
For testing, here are some nucleotide
and peptide sequences.
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Instructions: choose a blast program and e-value, then paste your FASTA sequences.
Note: "Collapse HSPs within this range" applies to blastn and tblastn; see '?' for more information.
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- FAQs
- What's a "pseudochromosome"?
The pseudochromosomes are snapshots of genome sequence in chromosomes
in the ongoing Medicago truncatula genome sequencing project. They consist
of BAC sequences and sequence-contigs in approximate order, as determined
by marker locations. The genome sequence for the euchromatic space is
approximately half- to two-thirds completed, so there are many gaps,
and BAC and contig orientations have not yet been determined. New
pseudochromosomes are constructed weekly.
- What are the little gray and black lines on the chromosome images?
Black lines indicate sequence gaps; gray lines indicate boundaries between
overlapping BACs (overlap has been removed in these cases).
- What are the colored dots?
Each dot represents a Blast HSP below the specified E-value. Several HSPs
may correspond to one query sequence, so two dots don't necessarily indicate
two independent matches of the same sequence.
- What is CViT-blast?
CViT stands for "Chromosome Visualization Tool." CViT is a set of perl
and CGI scripts for flexibly visualizing features on chromosomes, and
particularly for visualizing whole genomes. The scripts are still under
development, but will be made publicly available when ready.
- Credits:
- CViT-blast: Atif Ahmed, Ethy Cannon and Steven Cannon (UMN).
- Pseudochromosome construction by Shelley Wang (UMN) and Foo Cheung (TIGR).
- All that sequence:
the sequencing teams at University of Oklahoma, TIGR, Sanger Institute, and Genoscope.
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