chosen

about hg18 & rheMac2
chosen | Nov 17, 2008 4:18:54 PM
http://genome-mirror.bscb.cornell.edu/cgi-bin/hgTracks?hgsid=1230&chromInfoPage=
hg18
Sequence name   Length (bp) including gaps  
chr1 247,249,719  
chr1_random 1,663,265  
chr2 242,951,149  
chr2_random 185,571  
chr3 199,501,827  
chr3_random 749,256  
chr4 191,273,063  
chr4_random 842,648  
chr5 180,857,866  
chr5_h2_hap1 1,794,870  
chr5_random 143,687  
chr6 170,899,992  
chr6_cox_hap1 4,731,698  
chr6_qbl_hap2 4,565,931  
chr6_random 1,875,562  
chr7 158,821,424  
chr7_random 549,659  
chr8 146,274,826  
chr8_random 943,810  
chr9 140,273,252  
chr9_random 1,146,434  
chr10 135,374,737  
chr10_random 113,275  
chr11 134,452,384  
chr11_random 215,294  
chr12 132,349,534  
chr13 114,142,980  
chr13_random 186,858  
chr14 106,368,585  
chr15 100,338,915  
chr15_random 784,346  
chr16 88,827,254  
chr16_random 105,485  
chr17 78,774,742  
chr17_random 2,617,613  
chr18 76,117,153  
chr18_random 4,262  
chr19 63,811,651  
chr19_random 301,858  
chr20 62,435,964  
chr21 46,944,323  
chr21_random 1,679,693  
chr22 49,691,432  
chr22_h2_hap1 63,661  
chr22_random 257,318  
chrX 154,913,754  
chrX_random 1,719,168  
chrY 57,772,954  
chrM 16,571  
Total 3,107,677,273


Assembly Details

The NCBI Build 36.1 reference sequence is considered to be "finished", a technical term indicating that the sequence is highly accurate (with fewer than one error per 10,000 bases) and highly contiguous (with the only remaining gaps corresponding to regions whose sequence cannot be reliably resolved with current technology). Future work on the reference sequence will focus on improving accuracy and reducing gaps in the sequence. Statistics for the Build 36.1 assembly can be found on the NCBI Build 36.1 Statistics web page.

This assembly contains four alternate haplotype regions:

  • chr22_h2_hap1 -- an alternate chromosome 22 assembly that contains the CYP2D6 gene (NT_113959.1). CYP2D6 is deleted in the reference assembly.
  • chr5_h2_hap1 -- a chromosome 5 alternate assembly of the SMN1 gene region (NT_113801.1, NT_113802.1).
  • chr6_cox_hap1 -- an A1-B8-DR3 alternate haplotype assembly of the chromosome 6 MHC region based on sequence data from the COX library (NT_113891.1).
  • chr6_qbl_hap2 -- an A26-B18-DR3 alternate haplotype assembly of the chromosome 6 MHC region based on sequence data from the QBL library (NT_113892.1, NT_113893.1, NT_113894.1, NT_113895.1, NT_113896.1, NT_113897.1).

See the Wellcome Trust Sanger Institute MHC Haplotype Project web site for additional information on the chr6 alternate haplotype assemblies.

The Y chromosome in this assembly contains two pseudoautosomal regions (PARs) at chrY:1-2709520 and chrY:57443438-57772954. These sequences were taken from the corresponding regions in the X chromosome and are exact duplications of the X chromosome sequences at chrX:1-2709520 and chrX:154584237-154913754, respectively.

For further information on NCBI Build 36.1, see the NCBI Build 36.1 release notes.

Bulk downloads of the data are available from the UCSC downloads server via ftp or http. We recommend that you use ftp or rsync for downloading large or multiple files.

The hg18 annotation tracks were generated by UCSC and collaborators worldwide. See the Credits page for a detailed list of the organizations and individuals who contributed to this release.

 

http://genome-mirror.bscb.cornell.edu/cgi-bin/hgTracks?hgsid=16&chromInfoPage=

rheMac2

Sequence name   Length (bp) including gaps  
chr1 228,252,215  
chr2 189,746,636  
chr3 196,418,989  
chr4 167,655,696  
chr5 182,086,969  
chr6 178,205,221  
chr7 169,801,366  
chr8 147,794,981  
chr9 133,323,859  
chr10 94,855,758  
chr11 134,511,895  
chr12 106,505,843  
chr13 138,028,943  
chr14 133,002,572  
chr15 110,119,387  
chr16 78,773,432  
chr17 94,452,569  
chr18 73,567,989  
chr19 64,391,591  
chr20 88,221,753  
chrX 153,947,521  
chrUr 440,886  
Total 2,864,106,071

Tag: Bioinformatics Biotech

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