Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • sinopnazo
    Junior Member
    • Jan 2013
    • 4

    #1

    How to create .fastq file?

    Hi everybody,

    I'm new member and I'm new to Bioinformatics too.
    I'm using bwa. 0.6.2. I've chr1.fa reference genome file.
    I don't know how to create the .fastq file corresponding to my
    reference file. Do you have any idea?

    Many thanks,
    Best,

    nazo
    Last edited by sinopnazo; 02-01-2013, 04:39 AM.
  • winsettz
    Member
    • Sep 2012
    • 91

    #2
    What sequencing platform are you using? What is the format of your sequencing data?

    Comment

    • sinopnazo
      Junior Member
      • Jan 2013
      • 4

      #3
      I couldn't understand the question, but I'm using human genome (hg19) and I downloaded chromFa.tar.gz file.
      I indexed human choromosome 1 in bwa, but I don't know how to align my fastq file to it. Because I couldn't create its fastq file.

      Comment

      • TonyBrooks
        Senior Member
        • Jun 2009
        • 303

        #4
        Your sequencing data is the fastq file.

        Comment

        • sinopnazo
          Junior Member
          • Jan 2013
          • 4

          #5
          Then I expressed myself completely wrong. I don't have sequencing data, I'm trying to have one. I only have chr1.fa.

          Comment

          • TonyBrooks
            Senior Member
            • Jun 2009
            • 303

            #6
            Try the ENA at EBI or the SRA at NCBI.

            Comment

            • mknut
              Member
              • Jul 2012
              • 23

              #7
              Right, let's start at the very beggining. I see that you have done a little bit of reading on the topic and I understand that it might be confusing. Firstly, I assume that you are trying to answer a specific question using bioinformatics. What is your question, what exactly do you want to investigate? The more information you include the more likely people here will be to help you. Secondly, FASTQ is a format that stores your sequence and its quality score. Read the wiki page, link above. It is possible to download publicly available sequences from e.g. for human http://www.ncbi.nlm.nih.gov/Traces/s...obj&term=human They use .sra format, which you will have to convert to FASTQ using sra toolkit. Explanation - http://www.ncbi.nlm.nih.gov/books/NBK56562/ However, I would advise against downloading any of these sequences until you know exactly what you are trying to do. http://www.csc.fi/english/csc/course...e/ngs_workshop - this is a good resource for some basic information. If you find it too difficult, you can start with this workshop http://www.bioinf.uni-leipzig.de/~da...p_evop2012.pdf and wikipedia.

              Comment

              • sinopnazo
                Junior Member
                • Jan 2013
                • 4

                #8
                Thank you so much.

                It seems a lot of things to do...
                I'll try sra toolkit.

                Best,
                nazo.

                Comment

                Latest Articles

                Collapse

                • SEQadmin2
                  Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
                  by SEQadmin2



                  CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

                  Despite this, “CRISPR helped turn genome editing from a specialized technique into
                  ...
                  07-31-2026, 11:01 AM
                • SEQadmin2
                  Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
                  by SEQadmin2


                  Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

                  The systematic characterization of the human proteome has
                  ...
                  07-20-2026, 11:48 AM
                • 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

                ad_right_rmr

                Collapse

                News

                Collapse

                Topics Statistics Last Post
                Started by SEQadmin2, 08-03-2026, 10:13 AM
                0 responses
                15 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-31-2026, 02:55 AM
                0 responses
                32 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-24-2026, 12:17 PM
                0 responses
                23 views
                0 reactions
                Last Post SEQadmin2  
                Started by SEQadmin2, 07-23-2026, 11:41 AM
                0 responses
                21 views
                0 reactions
                Last Post SEQadmin2  
                Working...