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Thread | Thread Starter | Forum | Replies | Last Post |
Genomatix RNA-Seq workflow | rebrendi | Bioinformatics | 1 | 02-13-2012 08:13 AM |
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Barcoded PE adapters for multiplexing up to 12 samples | Pepe | Illumina/Solexa | 9 | 01-28-2010 05:36 PM |
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#1 |
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Location: Missouri Join Date: Apr 2010
Posts: 39
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Hello,
I am working with RNA-seq Illumina data files in Galaxy (http://main.g2.bx.psu.edu/). The files are 100bp paired-end reads, multiplexed with barcoding to distinguish samples. There are two files, one for each end of the paired-end reads (first three reads of the files are pasted below). The barcodes are the first four bases of the sequences in the s_7_1_sequence.txt file. Would the following Galaxy workflow be correct? 1. Upload both s_7_1_sequence.txt and s_7_2_sequence.txt to Galaxy with the reference genome selected 2. Run NGS: QC and manipulation --> FASTQ Groomer on each file to convert to Sanger FASTQ 3. Run NGS: QC and manipulation --> FASTQ joiner to combine the data from the two files 4. Run FASTX-TOOLKIT FOR FASTQ DATA --> Barcode Splitter to generate separate FASTQ files for each barcode group 5. Run NGS: RNA Analysis --> Tophat to map the reads from each group to the reference genome The problem I am having is that if I select paired-end for the library in Tophat, it requests two FASTQ files. Would I have to use FASTQ Splitter to separate the joined FASTQ files? I would be very appreciative of any suggestions. Thanks very much in advance, jjw File 1: s_7_1_sequence.txt @HWI-ST538_0096:7:1:1443:1917#0/1 CGTTNCAGACTCTGCAACGACAGCCTGCCCCCCGGCACCGTGAAGCTCTAGGCACGGCCTGCTCGCCGCCCGGGGACAAGGACTCCTGCCGCTGCCCCCG +HWI-ST538_0096:7:1:1443:1917#0/1 aaa`BcccccggggggfgggfgagggggdaggggggcegedeaadaggdegeeggdebgdZccc]Z`Z^c`S__[^_`aO_Zc^cd`Y`dBBBBBBBBBB @HWI-ST538_0096:7:1:1468:1938#0/1 ACGTNGTCTGTGATGCCCTTAGATGTCCGGGGCTGCACGCGCGCTACACTGACTGGCTCAGCGTGTGCCTACCCTACGCCGGCAGGGGCGGGGAACCCCC +HWI-ST538_0096:7:1:1468:1938#0/1 `_`^Bb_babegggggggggceeeedeggddeggeggegeeedeeeeegddeddccVacVX\ZSXXSX_Xb_XbBBBBBBBBBBBBBBBBBBBBBBBBBB @HWI-ST538_0096:7:1:1484:1983#0/1 AAAGTAGCAAATACACAGCATGAGAAATCGGCATCGGATGTCACAGGGAAAGTAGCAAACACACAGCATGAGAAATCAGCATCGGTTGTCACAGAGAAAG +HWI-ST538_0096:7:1:1484:1983#0/1 gggggfggegfggeggfgggggegggggeggefggggegg\dd^dadc]dda\dcddecZb[b`e_^]_\bbbee`TdY^_Y^BBBBBBBBBBBBBBBBB File 2: s_7_2_sequence.txt @HWI-ST538_0096:7:1:1443:1917#0/2 CGTTGGCAGCAGGCAGAGGTGGTGCAGTGGCAGCGGCAGGGGGCCTTGTCCCCGGGCGGCGGGCAGGCGCGGCCCCAGGCGTTACGGGGGCCGGGGGGGG +HWI-ST538_0096:7:1:1443:1917#0/2 ggggggggggggdgegcgaahebfefebbeecfabcaX`cBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB @HWI-ST538_0096:7:1:1468:1938#0/2 ACGTTGGGAATTCCTCGTTCATGGGGAATAATTGCAATCCCCGATCCCCATCACGAATGGGGTTCAACGGGTTACCCGCGCCTGCCGGCGTAGGGTAGGA +HWI-ST538_0096:7:1:1468:1938#0/2 gggggggggggggggggggdgggggeedegggadbffedb[dedddcecdgaehefegfdeebcdfadecacafPbb`Lbbd_ZdUX^BBBBBBBBBBBB @HWI-ST538_0096:7:1:1484:1983#0/2 TTTCCCCATGACATCCGATGCTGATTTCTCATGCTGTGCGTTTGCTACTTTCTCTGTGACAACCGATGCTGATTTCTCATGCTGTGTGTTTGCTACTTTC +HWI-ST538_0096:7:1:1484:1983#0/2 gggggggggggggggggggggggbgggedggggggeagefegbgdgaeeggggfgcgfegagggggegg`aad_fee_bgdddd^cX`caQX[M[bce`c |
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