Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • bi_maniac
    Member
    • Mar 2014
    • 30

    #31
    My histogram has 2 peaks in 149-150 and 200

    #Mean 166,846
    #Median 151
    #Mode 200
    #STDev 28,597
    #PercentOfPairs 16,089
    #InsertSize Count
    51 1
    57 1
    69 3
    73 1
    75 1
    76 1
    79 1
    82 2
    86 1
    87 1
    88 1
    91 1
    92 1
    95 1
    96 1
    97 1
    98 4
    101 1
    103 3
    105 1
    106 4
    107 2
    109 2
    111 3
    112 4
    113 2
    114 3
    115 9
    116 6
    117 3
    118 13
    119 3
    120 4
    121 17
    122 3
    123 8
    124 18
    125 12
    126 15
    127 16
    128 10
    129 13
    130 16
    131 8
    132 12
    133 17
    134 19
    135 16
    136 26
    137 25
    138 18
    139 48
    140 31
    141 32
    142 39
    143 35
    144 49
    145 53
    146 98
    147 160
    148 217
    149 398
    150 379
    151 240
    152 175
    153 114
    154 57
    155 32
    156 17
    157 8
    158 5
    159 2
    160 2
    161 1
    162 1
    163 1
    164 1
    165 2
    166 1
    167 3
    168 4
    169 1
    170 2
    172 5
    175 1
    176 1
    177 3
    178 4
    179 2
    180 5
    181 5
    182 4
    183 12
    184 4
    185 7
    186 3
    187 7
    188 13
    189 14
    190 15
    191 18
    192 31
    193 37
    194 52
    195 79
    196 82
    197 92
    198 267
    199 170
    200 405
    201 154
    202 52
    203 31
    204 22
    205 6
    206 3
    207 3
    208 1
    209 1
    210 2
    211 3
    214 1
    216 1
    217 3
    218 1
    221 4
    231 1
    238 1
    240 1
    241 2
    249 1
    256 1
    257 1
    260 2
    263 3
    264 2
    265 2
    266 2
    273 1
    282 3
    284 2
    286 2
    287 2
    288 2
    289 2
    290 1
    291 3
    292 1

    Comment

    • Brian Bushnell
      Super Moderator
      • Jan 2014
      • 2709

      #32
      That would be very strange, for random shearing. Is it an amplicon library? If so, my previous post is irrelevant, it was based on the assumption of random shearing. Note that BBMerge can merge reads with insert size longer than read length using kmer counting, but that won't work for amplicons, only random fragmentation with sufficient coverage (>5x or so). Sometimes you can increase the merge rate by quality trimming (flags "qtrim2=r trimq=12" in BBMerge, which will only trim if the initial merge attempt fails), and for generating an insert size histogram of very low quality reads, I generally use the "xloose" flag which makes it more sensitive (at the expense of false positive merges).

      What's the read quality like? Can you post the per-base qscore histogram? (reformat.sh in=reads.fq qhist=qhist.txt).

      Comment

      • bi_maniac
        Member
        • Mar 2014
        • 30

        #33
        Dear Brian.

        I will continue giving you more info as soon as I get it.

        Meanwhile let my give you many thanks for your most valuable help. Besides that I want to ask you for a further help:

        Do you know any tutorial or book that I could read in order to learn thiese concepts. The bioinformatics books I have are too basic and do not treat these issues.

        Comment

        • Brian Bushnell
          Super Moderator
          • Jan 2014
          • 2709

          #34
          Originally posted by bi_maniac View Post
          Do you know any tutorial or book that I could read in order to learn these concepts. The bioinformatics books I have are too basic and do not treat these issues.
          Sorry, I can't give you any advice there. Bioinformatics too rapidly-evolving now for books to be relevant for very long, I think.

          Comment

          • bi_maniac
            Member
            • Mar 2014
            • 30

            #35
            Hi Brian,

            It is amplicon library. Insert range is 300-370. I will send you exec reports soon.

            Comment

            • bi_maniac
              Member
              • Mar 2014
              • 30

              #36
              Hi, helpful people: this conversation continues here: http://seqanswers.com/forums/showthread.php?t=63930

              Thanks a lot.
              Last edited by bi_maniac; 11-02-2015, 11:55 AM.

              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, Yesterday, 07:41 AM
              0 responses
              12 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 08-03-2026, 10:13 AM
              0 responses
              25 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 07-31-2026, 02:55 AM
              0 responses
              38 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 07-24-2026, 12:17 PM
              0 responses
              25 views
              0 reactions
              Last Post SEQadmin2  
              Working...