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CHM13 human reference genome issue tracking

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CHM13-issues

CHM13 human reference genome issue tracking

For any downstream analysis, please use the following files:

  • Possible consensus or mis-assembly issue: <ver.>_issues.bed
  • Het sites: <ver.>/chm13.draft_<ver.>.curated_sv.20210612.vcf, <ver.>/chm13.draft_<ver.>.hets_combined.20210615.bed

Releases

  • 2021-10-13 Het regions lifted over from v1.0 to v1.1
  • 2021-06-23 Updating 3 additional issues and adding error k-mers in v1.0 and v1.1
  • 2021-06-15 Validated het SVs and clusters of heterozygous sites in v1.0 assembly
  • 2021-04-28 Issues track for HiFi and ONT read alignments from Winnowmap 2.01
  • 2021-03-08 Combined low coverage and clipped regions
  • 2021-02-23 Low coverage regions for HiFi, CLR, and ONT read alignments

Issues.bed file format

Label Description R,G,B Color
Low Low coverage 204,0,0 red
Low_Qual Low coverage from lower consensus quality 204,0,0 red
Error_Kmer K-mers identified as errors from the Illumina-HiFi hybrid 21-mers 0,0,0 black
Collapse Approximate region conatining sequence collapse 204,0,0 red
Chimeric_Hap Chimeric consensus of two haplotypes 204,0,0 red

Methods

Brief descriptions are provided for

More details will be provided in T2T-Polish.

Citation

Please cite the papers below if any of the materials posted on this github are used:

Mc Cartney AM, Shafin K, Alonge M et al., Chasing perfection: validation and polishing strategies for telomere-to-telomere genome assemblies. bioRxiv (2021) https://doi.org/10.1101/2021.07.02.450803

Nurk, Koren, Rhie, and Rautiainen et al., The complete sequence of a human genome. bioRxiv (2021) https://doi.org/10.1101/2021.05.26.445798

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CHM13 human reference genome issue tracking

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