Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Manual vs Blast2go annotation

    I have recently finished my transcriptome assembly and currently in the process of annotating ~50k transcripts. For annotating, i thought of using two approaches....

    Blasting those transcripts against closely related well annotated sp (in this Arabidopsis) and pull out the GO terms for the best hits from the blast and assign those GOs to my transcripts.

    Blasting those transcripts against Plant Refseq database and then use b2go pipeline to annotate them using default parameters in mapping and GO annotation stepS.

    Now i am wondering how do i compare which of the annotation is best. These are the following i can think of:

    a) How many transcripts that were annotated in the finally annotation.

    b) How many transcripts that have GOs that are associated with "BP" term

    c) Evidence Code distribution for hits and sequences of the GO terms for those transcripts.

    What do you think of these criteria and what else i should be thinking of before deciding which annotation i should be selecting in the end.

  • #2
    Hi -

    You could calculate those statistics but unless you know what 'good values' are for the statistics you won't really be able to evaluate the performance of the annotation method. For example, you may ask, "How many transcripts were annotated?" and you may think that the method that annotates the most transcripts is the best, but in fact there could be a lot of false positive annotations. Incorrect annotations are as bad as no annotations when it comes time to interpret your results.

    What you need are a set of similar transcripts that already have high quality GO annotations that you can use to evaluate different annotation methods. You can compare the results of the annotations that are output by the various methods and ask how similar they are to the original ones. There are a lot of different statistics you can calculate: precision, recall, sensitivity, specificity, etc. You could start by simply calculating the number of true positive and false positives and true negative and false negatives.

    That said, if you have a closely related species, its pretty common to simply transfer the annotations from the best blast hit to your transcript. I'd be careful to use strict parameters in the blast search.

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Essential Discoveries and Tools in Epitranscriptomics
      by seqadmin


      The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist on Modified Bases...
      Yesterday, 07:01 AM
    • seqadmin
      Current Approaches to Protein Sequencing
      by seqadmin


      Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
      04-04-2024, 04:25 PM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    55 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    51 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    45 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    55 views
    0 likes
    Last Post seqadmin  
    Working...
    X