Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Who let M's and R's in the Genome

    Just looking for other peoples input on something

    Has anyone notice there are two R and one M IUPAC codes on chromosome 3 in the reference genomes, both NCBI36 and GRCh37. Maybe not surprisingly they sit in the FHIT gene.

    Does this worry anyone for genome indexing or the such, seems minor in 3/3billion.
    Attached Files

  • #2
    Yes I noticed that, they are quite odd... I just replace them with N's when doing analysis.
    SpliceMap: De novo detection of splice junctions from RNA-seq
    Download SpliceMap Comment here

    Comment


    • #3
      Surprisingly, I noticed this yesterday too!
      Not expected, but no clue if it affects things downstream...
      --
      bioinfosm

      Comment


      • #4
        I know in some cases they use N to mask sequence that are repeats.

        Comment


        • #5
          the other letters in the code

          m= a or c, as in amino

          r= g or a, as in purine

          n= a or g or c or t/u, unknown, or other

          Comment


          • #6
            Originally posted by Joann View Post
            m= a or c, as in amino

            r= g or a, as in purine

            n= a or g or c or t/u, unknown, or other
            ah ha, good to know, thanks!

            Comment


            • #7
              Wait! there's more...

              Please see Annex C, Appendix 2, Table 1, page 16 at, for example,

              http://www.noip.gov.vn/noip/resource.nsf/vwResourceList/B4F5E35FA26A8AA4472577360013F1D3/$FILE/Standards%20%E2%80%93%20ST25.pdf

              for a complete list of nucleotide letter symbols in use per a current international standard.

              See also
              An extended IUPAC nomenclature code for polymorphic
              nucleic acids
              doi:10.1093/bioinformatics/btq098
              Last edited by Joann; 01-21-2011, 02:09 PM. Reason: update

              Comment


              • #8
                Interesting to know something apart from A,T,G,C,N.

                But UCSC has them as "N"s

                Comment


                • #9
                  These additional letters are sometimes called 'ambiguiety codes'. Back in the day when a 30X human genome sequence cost a billion dollars instead of several thousand, every piece of sequence information was much more precious. Knowing a position was a purine was better than calling it an N. The codes are also useful for reporting heterozygous genotype information as a single letter. The fact that they still occur in reference genomes is mostly just a nuisance for bioinformatics and thus some resources such as UCSC convert them to N's. I believe human genome sequences retrieved via Ensembl may still contain them though.

                  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
                  26 views
                  0 likes
                  Last Post seqadmin  
                  Started by seqadmin, 12-13-2024, 08:24 AM
                  0 responses
                  42 views
                  0 likes
                  Last Post seqadmin  
                  Started by seqadmin, 12-12-2024, 07:41 AM
                  0 responses
                  28 views
                  0 likes
                  Last Post seqadmin  
                  Started by seqadmin, 12-11-2024, 07:45 AM
                  0 responses
                  42 views
                  0 likes
                  Last Post seqadmin  
                  Working...
                  X