Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Any tricks? 244 sample SampleSheet.csv using NextSeq?

    We are sequencing a pool of 244 samples on our new (now obsolete?) NextSeq500. First time with over 96 samples. Can we just make one SampleSheet.csv with the 244 samples and their indecies (indexes?), and, will the bcl2fastq.pl script work? *Note* The bcl2fastq.pl script is being "managed" by the HPC center, so I didn't install it, and honestly don't know much about it yet.

    Thanks!

    -p

  • #2
    Yes. Use Illumina experiment manager (windows only, download from Illumina) to make the samplesheet (if you don't have a prior example). I have done 9000+ samples in a single sheet without any problems as long as your indexes have no collisions/sample names are in right format (no space, odd characters etc).

    Comment


    • #3
      Originally posted by GenoMax View Post
      Yes. Use Illumina experiment manager (windows only, download from Illumina) to make the samplesheet (if you don't have a prior example). I have done 9000+ samples in a single sheet without any problems as long as your indexes have no collisions/sample names are in right format (no space, odd characters etc).
      Great, thanks. We have IEM and should be able to handle the index names.

      Comment


      • #4
        Remember to run dos2unix on SampleSheet.csv if you move the samplesheet directly from your PC to the server otherwise you should be all set.

        Comment


        • #5
          Hmmm,
          Actually, the IEM only gives me the option of 96-well plates. Do we need to manually create a new 384-well plate file first? Or use a HiSeq option?

          Comment


          • #6
            Use create SampleSheet option on main screen and then NextSeq. It may be painful to do 244 rows this way though. You could just get a sample and then edit outside IEM.

            Comment


            • #7
              Originally posted by GenoMax View Post
              Use create SampleSheet option on main screen and then NextSeq. It may be painful to do 244 rows this way though. You could just get a sample and then edit outside IEM.
              Tried both ways. Nope. I can't figure it out. IEM accepts the SamplePrepKit file with 384 wells. But when I try to load a plate with 384 wells I get an error saying "Index was outside the bounds of the array". I've made custom plates and assays before.

              Anyone with a NextSeq have a 384-well SampleSheet, or plate file, that works?

              Calling Illumina now...

              *EDIT* I was able to add rows to the SampleSheet manually from within IEM. I could never get a plate to load or edit with 384 wells. It was a PITA but now I have a Sample template to work with. Still don't know if it'll work but according to GenoMax, it should. Thanks.
              Last edited by hoytpr; 07-20-2017, 12:57 PM. Reason: Want to be clear and correct.

              Comment


              • #8
                Your samplesheet does not need to be generated by IEM.
                IEM is a nice tool, so you get the headers, parameters etc right.

                But you can also easily open the resulting .csv in excel and add how many rows you wish.
                Last edited by Genetic Librarian; 07-26-2017, 04:43 AM.

                Comment


                • #9
                  Just wanted to thank y'all for your help. All 200+ samples processed perfectly on the first try.

                  Comment

                  Latest Articles

                  Collapse

                  • seqadmin
                    Recent Advances in Sequencing Analysis Tools
                    by seqadmin


                    The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
                    Today, 07:48 AM
                  • seqadmin
                    Essential Discoveries and Tools in Epitranscriptomics
                    by seqadmin




                    The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
                    04-22-2024, 07:01 AM

                  ad_right_rmr

                  Collapse

                  News

                  Collapse

                  Topics Statistics Last Post
                  Started by seqadmin, Today, 07:17 AM
                  0 responses
                  11 views
                  0 likes
                  Last Post seqadmin  
                  Started by seqadmin, 05-02-2024, 08:06 AM
                  0 responses
                  19 views
                  0 likes
                  Last Post seqadmin  
                  Started by seqadmin, 04-30-2024, 12:17 PM
                  0 responses
                  20 views
                  0 likes
                  Last Post seqadmin  
                  Started by seqadmin, 04-29-2024, 10:49 AM
                  0 responses
                  28 views
                  0 likes
                  Last Post seqadmin  
                  Working...
                  X