Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • SnpEff matching policy

    Hi there,

    I'm digging a little bit into SnpEff and everything works fine, but I have a doubt for which I didn't find an answer in any of the SnpEff papers/documentation.
    I have a variant (rs4372192 ) in the intronic region of one gene (SAMD11) and it returns the annotations for all Ensembl non protein-coding transcripts in an interval of +/-5KB from this variant. Everything fine up to here.
    But, not all the protein-coding transcripts for the gene (SAMD11) are matched, only one. Why is it not returning all protein-coding transcripts? Anybody knows if this is configurable? But, in any case is there any reason I should know for this working.

    SnpEff output:
    Code:
    EFF=DOWNSTREAM(MODIFIER||||NOC2L|processed_transcript|CODING|ENST00000327044|),DOWNSTREAM(MODIFIER||||NOC2L|processed_transcript|CODING|ENST00000477976|),DOWNSTREAM(MODIFIER||||NOC2L|processed_transcript|CODING|ENST00000483767|),DOWNSTREAM(MODIFIER||||NOC2L|processed_transcript|CODING|ENST00000496938|),DOWNSTREAM(MODIFIER||||SAMD11|protein_coding|CODING|ENST00000420190|),INTRON(MODIFIER||||SAMD11|protein_coding|CODING|ENST00000342066|),TRANSCRIPT(MODIFIER||||SAMD11|protein_coding|CODING|ENST00000474461|),TRANSCRIPT(MODIFIER||||SAMD11|protein_coding|CODING|ENST00000478729|),UPSTREAM(MODIFIER||||SAMD11|protein_coding|CODING|ENST00000464948|),UPSTREAM(MODIFIER||||SAMD11|protein_coding|CODING|ENST00000466827|)
    Ensembl visualization:
    http://www.ensembl.org/Homo_sapiens/...01cce786943248


    Cheers,

    Pablo.

  • #2
    I will answer myself
    A clue for this might be that the non-matched transcripts are marked as novel in Ensemble, instead of known. So, there are two alternatives: first, that the database SnpEff is using does not include these transcripts; or second that they are filtered out as they are less confident.

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Advancing Precision Medicine for Rare Diseases in Children
      by seqadmin




      Many organizations study rare diseases, but few have a mission as impactful as Rady Children’s Institute for Genomic Medicine (RCIGM). “We are all about changing outcomes for children,” explained Dr. Stephen Kingsmore, President and CEO of the group. The institute’s initial goal was to provide rapid diagnoses for critically ill children and shorten their diagnostic odyssey, a term used to describe the long and arduous process it takes patients to obtain an accurate...
      12-16-2024, 07:57 AM
    • seqadmin
      Recent Advances in Sequencing Technologies
      by seqadmin



      Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.

      Long-Read Sequencing
      Long-read sequencing has seen remarkable advancements,...
      12-02-2024, 01:49 PM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, 12-17-2024, 10:28 AM
    0 responses
    33 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 12-13-2024, 08:24 AM
    0 responses
    49 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 12-12-2024, 07:41 AM
    0 responses
    34 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 12-11-2024, 07:45 AM
    0 responses
    46 views
    0 likes
    Last Post seqadmin  
    Working...
    X