Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • ddunbar
    Junior Member
    • May 2013
    • 2

    Identifying unique aptamer sequences

    Hello all.
    A biologist colleague has generated sequencing libraries based on a SELEX type of enrichment of artificial aptamers that have bound to bacterial cells. He will have Ion Torrent sequence (short read, single end) output (millions of reads per sample) and would like help with identifying sequences that uniquely or preferentially bind each bacterial strain. The aptamers are 80 nucleotides long and are generated randomly. There are several rounds of enrichment, so there will be sequences represented multiple times. Biological replicates will help find true positives.

    Ideally he would find sequences that are present exclusively in each bacterial strain's bound aptamer population. Initially we'll look at the full length aptamers but of course specific motifs present in different aptamers may be enriched.

    Does anyone know if there is a Bioconductor (or other) package that will already do this kind of counting short reads and comparing between samples?

    This can be done in Perl, for example, using hashes and counting each sequence (and potentially each kmer in the reads) but I suspect there will be a better way to do it. We don't wan to reinvent the wheel and would like to reuse anyone's good ideas and code.

    Any help or thoughts would be greatly appreciated.

    Donald
  • dawe
    Senior Member
    • Apr 2009
    • 258

    #2
    You may deal with aptamer sequences using only bash utilities with grep, awk, sort and uniq.
    First of all you have to put all sequences (one per line) in a file, then

    $ sort file | uniq -c | sort -k1,1n > counted_sequences

    You will end up with hundreds (or thousands) out of millions with a power law enrichment count.
    Once you have all files, counted, it's easy with grep to check counts across SELEX cycles or samples.

    HTH

    Comment

    • ddunbar
      Junior Member
      • May 2013
      • 2

      #3
      Many thanks for that dawe. Works nicely.
      Best wishes,
      Donald

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
        by SEQadmin2



        Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
        ...
        07-09-2026, 11:10 AM
      • SEQadmin2
        Cancer Drug Resistance: The Lingering Barrier to Rising Survival
        by SEQadmin2



        Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

        There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
        07-08-2026, 05:17 AM
      • GATTACAT
        Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
        by GATTACAT
        Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
        07-01-2026, 11:43 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 07-13-2026, 10:26 AM
      0 responses
      22 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-09-2026, 10:04 AM
      0 responses
      32 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-08-2026, 10:08 AM
      0 responses
      20 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-07-2026, 11:05 AM
      0 responses
      34 views
      0 reactions
      Last Post SEQadmin2  
      Working...