Hi:

I know from the website (http://genome.ucsc.edu/FAQ/FAQdownloads#download10) 
that random fasta files associated with chromosomes are data data related to 
sequence that is known to be in a particular chromosome, but could not be 
reliably ordered within the current sequence and now also for sequences that is 
not in a finished state, but whose location in the chromosome is known, in 
addition to the unordered sequence.

However, I am interested in determining contig info for sequence matches to the 
random files associated with chromosomes. Specifically, is there a table 
matching e.g. chr1_random to different NCBI identifiers (e.g. NT_004434.18)? 
Would chr1_random be ONE contig or conglomerate of all unmatching contigs 
associated with chr1?

thanks for you assistance.

Jimmy
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