Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • First Question

    Hello, I am a new graduate student and I am hoping to be able to do some sequence analysis, but here is the problem: I have never done anything like this before and I don't know anyone with the experience. So I am hoping this forum can help me.

    I want to investigate some genomic data that is present in an sra file. I am specifically looking for sequences similar to a gene with a known full cDNA sequence. How can I do this? what software do I need? Is it even possible?

    If anyone can help that would be great

    Also, nice to meet you

  • #2
    Everything is possible. The question is what skills you have to make it possible. Can you write small perl codes? Can you download and install readily available programs?

    Many aspects of your question are not clear from the short description. Are you trying to find SNPs? Are you trying to find genes in a related organism? So, let me create one example and answer it. Let us say you have a SRA file with Illumina gene (RNAseq) data from one organism (one type of mosquito - A) and you have full length cDNA from a related organism (different type of mosquito - B). You want to figure out the homologous gene in mosquito A.

    In that case, you can use Bowtie to align all RNAseq reads to the cDNA, and then assemble the matching reads with any simple program like cap3.

    You can see that I made many assumptions in the above description. Any change in the assumption (let's say 454 data instead of Illumina) will change the answer. So you have to be more specific.

    You may read some of the descriptions in these commentaries (http://www.homolog.us/blogs/category/introductory-2/) to learn about wide variety of analysis tools and skills that all fall under bioinformatics. It is not all about finding programs, downloading and running.
    http://homolog.us

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Choosing Between NGS and qPCR
      by seqadmin



      Next-generation sequencing (NGS) and quantitative polymerase chain reaction (qPCR) are essential techniques for investigating the genome, transcriptome, and epigenome. In many cases, choosing the appropriate technique is straightforward, but in others, it can be more challenging to determine the most effective option. A simple distinction is that smaller, more focused projects are typically better suited for qPCR, while larger, more complex datasets benefit from NGS. However,...
      10-18-2024, 07:11 AM
    • seqadmin
      Non-Coding RNA Research and Technologies
      by seqadmin




      Non-coding RNAs (ncRNAs) do not code for proteins but play important roles in numerous cellular processes including gene silencing, developmental pathways, and more. There are numerous types including microRNA (miRNA), long ncRNA (lncRNA), circular RNA (circRNA), and more. In this article, we discuss innovative ncRNA research and explore recent technological advancements that improve the study of ncRNAs.

      Nobel Prize for MicroRNA Discovery
      This week,...
      10-07-2024, 08:07 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, 10-17-2024, 07:29 AM
    0 responses
    49 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 10-15-2024, 06:35 AM
    0 responses
    37 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 10-14-2024, 02:44 PM
    0 responses
    39 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 10-11-2024, 06:55 AM
    0 responses
    26 views
    0 likes
    Last Post seqadmin  
    Working...
    X