This track shows "reciprocal best" alignments of $o_organism ($o_db, $o_date) to the $organism genome. These alignments were generated using blastz and blat alignments of $o_organism genomic sequence from the Nov. 2003 Arachne draft assembly. Alignments were made using a gap scoring system that allows longer gaps than traditional affine gap scoring systems. It can also tolerate gaps in both $o_organism and $organism simultaneously. These "double-sided" gaps can be caused by local inversions and overlapping deletions in both species.
The chain track displays boxes joined together by either single or double lines. The boxes represent aligning regions. Single lines indicate gaps that are largely due to a deletion in the $o_organism assembly or an insertion in the $organism assembly. Double lines represent more complex gaps that involve substantial sequence in both species. This may result from inversions, overlapping deletions, an abundance of local mutation, or an unsequenced gap in one species. In cases where multiple chains align over a particular region of the $organism genome, the chains with single-lined gaps are often due to processed pseudogenes, while chains with double-lined gaps are more often due to paralogs and unprocessed pseudogenes.
In the "pack" and "full" display modes, the individual feature names indicate the chromosome, strand, and location (in thousands) of the match for each matching alignment.
The alignments were generated by blastz on repeatmasked sequence using the following $organism/$o_organism scoring matrix:
A C G T A 100 -300 -150 -300
C -300 100 -300 -150 G -150 -300 100 -300
T -300 -150 -300 100
K = 4500, L = 3000, Y = 3400, H = 2000
The resulting alignments were fed into axtChain, which organizes all alignments between a single $o_organism chromosome and a single $organism chromosome into a group and creates a kd-tree out of the gapless subsections (blocks) of the alignments. A dynamic program was then run over the kd-trees to find the maximally scoring chains of these blocks. Chains scoring below a threshold were discarded.
To place additional chimp sequences not initially aligned by blastz, a DNA blat of the unmasked sequence was performed. The resulting blat alignments were also chained and then merged with the blastz-based chains from the previous step to produce a set of "all chains".
Due to the draft nature of this initial genome assembly, the chain track and the companion net track were generated using a "reciprocal best" strategy. This strategy attempts to minimize paralog fill-in for missing orthologous chimp sequence by filtering out of the human net all sequences not on the chimp side of the net.
First, the merged blastz and blat chains were used to generate an alignment net using the program chainNet (described on the Chimp Recip Net track description page). Next, the subset of chains in the chimp-reference net were extracted and used for an additional netting step. The resulting human-reference net was used to generate the reciprocal best Chimp Recip Net browser track. Non-syntenic sequences smaller than 50 bases were filtered out. Chains extracted from this net are displayed on the Chimp Recip Chain browser track.
The $o_organism sequence used in this track was obtained from the 13 Nov. 2003 Arachne assembly. We'd like to thank the National Human Genome Research Institute (NHGRI), the Broad Institute at MIT/Harvard, and Washington University St. Louis School of Medicine for providing this sequence.
Blastz was developed at Pennsylvania State University by Scott Schwartz, Zheng Zhang, and Webb Miller with advice from Ross Hardison.
Lineage-specific repeats were identified by Arian Smit and his RepeatMasker program.
The axtChain program was developed at the University of California at Santa Cruz by Jim Kent with advice from Webb Miller and David Haussler.
The browser display and database storage of the chains were generated by Robert Baertsch and Jim Kent.
Chiaromonte, F., Yap, V.B., Miller, W. Scoring pairwise genomic sequence alignments. Pac Symp Biocomput 2002, 115-26 (2002).
Kent, W.J., Baertsch, R., Hinrichs, A., Miller, W., and Haussler, D. Evolution's cauldron: Duplication, deletion, and rearrangement in the mouse and human genomes. Proc Natl Acad Sci USA 100(20), 11484-11489 (2003).
Schwartz, S., Kent, W.J., Smit, A., Zhang, Z., Baertsch, R., Hardison, R., Haussler, D., and Miller, W. Human-Mouse Alignments with BLASTZ. Genome Res. 13(1), 103-7 (2003).