Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • genome_anawk1
    Junior Member
    • May 2011
    • 7

    bfast for analyzing AB's SOLiD data

    Dear Bfast experts and users,

    I have 4 questions and hope to seek some answers from the community. My questions are interspersed in the bfast workflow described in two parts below.

    PART-1
    1- convert experimental data to bfast input (these are for mate-pair library preps).
    solid2fastq -n 500000 -o reads *.csfasta *.qual
    ("reads.j.fastq" , j=1...,N files created)

    Q1- Is this command right for mate-pair library prep.

    2- reference sequence to nucleotide space and color space
    bfast fasta2brg -f ref_genome.fa
    bfast fasta2brg -f ref_genome.fa -A 1

    3 - create 10 masks using information from manual
    generate 10 bif files (M=10)
    bfast index -f ref_genome.fa -m <mask> -w 14 -i <index number> -A 1

    10 is optimal for analyzing the human genome as suggested by the authors for bfast.
    Q2- Can anyone please suggest a number for the mouse genome? An approximate value would be good enough - say 15 or 50?

    I prefer not to compromise on sensitivity - so I prefer to use all indices to map short reads - part2 .. summarized below.

    PART-2
    1- bfast match
    bfast match -f ref_genome.fa -A 1 -r reads.<N>.fastq > bfast.matches.file.ref_genome.<N>.bmf

    2- bfast localalign
    bfast localalign -f ref_genome.fa -m bfast.matches.file.ref_genome.<N>.bmf -A 1 > bfast.aligned.file.ref_genome.<N>.baf

    3- bfast postprocess
    bfast postprocess -f ref_genome.fa -i bfast.aligned.file.ref_genome.<N>.baf -A 1 > bfast.reported.file.ref_genome.<N>.sam

    Q3- If I choose to split jobs for PART-2, for specific indices, Do I use bmfmerge after #1 and before #2 ?

    Q4 - With bmfmerge, What would be the cutoff / flag for reasonable analysis using the mouse genome? An example command would help please. It has been suggested that a value of "-M 500" may be useful when aligning the Human Genome. I would welcome any suggestions for the mouse genome.

    Hope you can please help,
    Thanks very much in advance,
    cheers,
    another new bfast analyzer.
    ---------------
  • nilshomer
    Nils Homer
    • Nov 2008
    • 1283

    #2
    Q1 - Looks good.
    Q2 - Use the ten provided; they should be sufficient.
    Q3 - Yes.
    Q4 - The "-M" option should match the value in "bfast match" and "bfast localalign". The defaults should match across commands.

    Comment

    Latest Articles

    Collapse

    • 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
    • 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

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, 07-24-2026, 12:17 PM
    0 responses
    19 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-23-2026, 11:41 AM
    0 responses
    18 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-20-2026, 11:10 AM
    0 responses
    25 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-13-2026, 10:26 AM
    0 responses
    38 views
    0 reactions
    Last Post SEQadmin2  
    Working...