Dinh/Dinh 2013/NOTES/2013-6-24: Difference between revisions
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* Obtain UMI from the first 10bp of read 1, label both reads with UMI | * Obtain UMI from the first 10bp of read 1, label both reads with UMI | ||
* Trim 27 bp from 5 prime end of read 1 and read 2 | * Trim 27 bp from 5 prime end of read 1 and read 2 | ||
* Remove adapter sequences using fastq-mcf | |||
* Create kmer_table for COPE | * Create kmer_table for COPE | ||
* Use COPE to combine overlapping read 1 and read 2 | * Use COPE to combine overlapping read 1 and read 2 |
Revision as of 00:32, 25 June 2013
Analysis of Blueprint MiSeq Test Run
- 2 X 250bp MiSeq PE run, total = 13,117,847 PE reads
- Noi's labnote page: http://genome-tech.ucsd.edu/LabNotes/index.php/Noi/NOTES/2013-6-6
Pre-processing
- Obtain UMI from the first 10bp of read 1, label both reads with UMI
- Trim 27 bp from 5 prime end of read 1 and read 2
- Remove adapter sequences using fastq-mcf
- Create kmer_table for COPE
- Use COPE to combine overlapping read 1 and read 2
for f in 1Index1_S1 1Index2_S2 1Index3_S3 2Index4_S6 1Index5_S4 2Index6_S7 2Index7_S8 1Index8_S5 do ./getUMI.pl 130620_MiSeq/TES1-${f}_L001_R1_001.fastq 130620_MiSeq/TES1-${f}_L001_R2_001.fastq $f ~/softwares/cope-src-v1.1.3/src/cope -a $f.R1.fq -b $f.R2.fq -o $f.fq -2 $f.leftR1.fq -3 $f.leftR2.fq -m 1 -t kmer_table.freq.cz -f kmer_table.freq.cz.len >cope.$f.log 2>cope.$f.error rm $f.R1.fq $f.R2.fq done
COPE results
index | total_pairs | connected_pairs | connect_ratio(%) | low_quality_pairs | low_quality_ratio(%) |
1 | 546,091 | 37,624 | 6.88969 | 239413 | 43.8412 |
2 | 1,201,482 | 76,332 | 6.35315 | 603335 | 50.2159 |
3 | 2,107,061 | 120,889 | 5.73733 | 1155859 | 54.8565 |
5 | 2,416,376 | 157,448 | 6.51587 | 1124046 | 46.5178 |
8 | 2,699,273 | 191,332 | 7.08828 | 1138412 | 42.1748 |
4 | 1,576,107 | 100,314 | 6.36467 | 805229 | 51.0897 |
6 | 2,025,366 | 131,396 | 6.48752 | 990421 | 48.9008 |
7 | 546,091 | 35,800 | 6.55568 | 239459 | 43.8497 |
Alignment with Bowtie2
- The long reads were not compatible with our pipeline using Bowtie2, because the aligner suppresses read name lines which are longer than 256 characters. This causes truncated original reads stored in the read name line.
- Added code to split long reads into multiple short reads to use Bowtie2
- Mapping pipeline:
cur_dir="/media/3TB_Dinh/Blueprint" reads_dir="/media/3TB_Dinh/Blueprint" email="diep.hue.dinh@gmail.com" bisReadMapper="/home/ddiep/scripts/MethylationPipeline/scripts/smartBisReadMapper.pl" template_fwd="/media/2TB_storeA/BisRef/bisHg19/hg19.fa.bis.fwd.bowtie2" template_rev="/media/2TB_storeA/BisRef/bisHg19/hg19.fa.bis.rev.bowtie2" template_fa="/media/2TB_storeA/BisRef/bisHg19/hg19.fa" soap="/home/ddiep/softwares/soap2.21release/soap" bowtie="bowtie2" cpg="/media/2TB_storeA/BisRef/bisHg19/C_Pos/hg19.fa.cpg.positions.txt" INDX="1Index1_S1 1Index2_S2 1Index3_S3 2Index4_S6 1Index5_S4 2Index6_S7 2Index7_S8 1Index8_S5" # make sure the qual_base variable is set correctly cd $cur_dir for s in ${INDX} do f="$s.fq" g="$s.leftR1.fq" h="$s.leftR2.fq" n="$s-MS" mkdir $n echo "cd $cur_dir/$n" > $n.job echo "$bisReadMapper -r $reads_dir/$f -W $template_fwd -C $template_rev -g $template_fa -a $bowtie -p 16 -b 33 -n $n.f1 -q 20 -l $cpg > $n.f1.statusMbias 2>$n.f1.err" >> $n.job echo "$bisReadMapper -r $reads_dir/$g -W $template_fwd -C $template_rev -g $template_fa -a $bowtie -p 16 -b 33 -n $n.f2 -q 20 -l $cpg > $n.f2.statusMbias 2>$n.f2.err" >> $n.job echo "$bisReadMapper -r $reads_dir/$h -W $template_fwd -C $template_rev -g $template_fa -a $bowtie -p 16 -b 33 -n $n.f3 -q 20 -l $cpg > $n.f3.statusMbias 2>$n.f3.err" >> $n.job echo "rm *encoded" >> $n.job done
Mapping statistics
Remove clonal reads
- Use prof. zhang's code to remove clonal reads using UMI