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4dn:phase1:working_groups:omics_data_standards:minutes-07-10-2017

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Omics Data Standards WG - Minutes 07-10-2017

Comparison of normalization methods

(Slides by Burak et al. available on wiki to explore different normalization schemes)

  • DCIC has followed through workflows and can now present normalization results in HiGlass and Juicer (links in Slides)
  • DCIC will be working on 6 samples in the next step and work with Ren lab for HiNorm procedures
  • Metrics used to compare normalization procedures
    • There are no accepted metrics, four used by ENCODE may not be applicable to HiC data and it seems the current best way is to visualize first
    • Biases may be a good metric. When results near the unmappable regions are shown it might differ from different normalization methods
  • Currently using published datasets (first 6), and DCIC is planning to include the 4DN datasets (submitted by Job, for example)
    • The reason why the 6 examples are chosen is that for a single cell type there can be different publications for comparison purposes
    • One big dataset from Job on HFF cells and some from Ren’s lab is pending. DCIC is planning to process 10 additional datasets
    • HFF data has 2 replicates and each has ~2B unmapped reads, which is the same for ES (making it ~8B in total)
  • DCIC needs to agree with the labs producing data about how they should be processed
  • The plan would be to have a look at the normalizations at those data
    • The current dataset is Rao et al. IMR90 datasets, it has the entire dataset but a smaller sample from the data.
    • We can compare this (diluted HiC) to in situ HiC data.
    • We need to make sure to make the in situ HiC data available to people before letting them view the data
      • This can be handled by Juicebox
      • DCIC is working on it

Optical mapping

Feng’s lab has performed optical mapping with a manuscript with Job’s lab in bioRxiv. This would be discussed in the next meeting.

It might be helpful to have the agenda in the email beforehand.

Discussion of genome support

  • DCIC has put up together a draft about the genome support (hg38 over hg19). The proposal can be seen at https://docs.google.com/document/d/1U_6LlEG7lFZjUv9xqw0U1u2JQRYWJ3rxAB0qDj8h55w/edit
  • What does GRCh38 is more “future proof” than hg19 mean?
    • GRCh38 would be using more and more, while hg19 less and less, so in the future, for example, three years, GRCh38 would be prevalent.
    • One thing is that infrastructure to support a new reference, it takes lots of time. While the genome assembly may continue to evolve (we may have GRCh39 in the future).
      • The key issue is that supporting multiple assemblies requires more work. There can be new assemblies but GRCh38 would be better than hg19 in the future if only one would be supported.
  • This policy has passed unanimously at this OMICS meeting and will be sent to Steering Committee.
    • This might affect other working groups, for example, the Imaging WG to design probes on the reference.
  • This resolution will also be highlighted in Joint Analysis Working Group meeting to make sure people know that this reference has become the standard for 4DN analysis.

HiGlass and domain calls

Standard protocols for other technologies

  • There are some technologies (for example, ATAC-seq) that may need protocols finalized by 4DN so that DCIC can start accepting those data. These protocols have been pretty much standardized and probably don’t need much discussion
  • People will be asked to submit such protocols to 4DN to proceed.
4dn/phase1/working_groups/omics_data_standards/minutes-07-10-2017.1550267262.txt.gz · Last modified: 2025/04/22 16:21 (external edit)