Sam:LabNotes/Microbiome-new/2010-12-8: Difference between revisions

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   4. Using the down-sampled reads: To draw bias-extent plot(This is to test the bias extent) (folder 4)
   4. Using the down-sampled reads: To draw bias-extent plot(This is to test the bias extent) (folder 4)


  Pair-end data analysis
  '''Pair-end data analysis'''
   1. Perform ABySS De Novo assembly, compare N50, Adjust K-mer
   1. Perform ABySS De Novo assembly, compare N50, Adjust K-mer
   2. Align AbySS contigs back to E.coli template using bowtie to assess mapping rate & coverage
   2. Align AbySS contigs back to E.coli template using bowtie to assess mapping rate & coverage
   3. Filter the read to >300bp and BLAST to nt.PE alignment using Bowtie to assess chimerics
   3. Filter the read to >300bp and BLAST to nt.PE alignment using Bowtie to assess chimerics

Revision as of 19:11, 13 December 2010

Data analysis of E.coli SAGs sequencing results(short and long amplified E.coli SAGs -3rd test 11-07-'10)

Background

  • Eight E.coli SAGs samples were made to Illumina sequencing libraries using (N2)Primer-based barcodes ID1 to ID8.
  • These libraries were equally pulled (20ng per library) and sequenced in pair-end(PE) mode.
  • The sequenced data processed by Dr. Zhang for base-calling and saved into FASTQ files.
  • Since I don't have genome-tech server permission, I asked Dinh's help to transfer data into Genemapster server.

Analysis approaches

Single-end data analysis

Perform whole reads Bowtie-mapping, genome coverage calculate (folder 1)
  1. Using the whole reads: Extracted the failed-to-aligned reads. Perform ABySS De Novo assembly, Filter out < 300bp contigs, Local Blast, Annotating the Blast results.(folder 3)
  2. Using the whole reads: Using the bowtie to do PE alignemt reads and figure out chimeric detection.

Downsampling the whole reads to where total specific (output=1) E.coli alignment reaches 1,000,000 reads 
  3. Using the down-sampled reads: To re-calculate the new genome coverage rate using the down-sampled reads number (folder 2)(This is to test the bias extent)
  4. Using the down-sampled reads: To draw bias-extent plot(This is to test the bias extent) (folder 4)
Pair-end data analysis
  1. Perform ABySS De Novo assembly, compare N50, Adjust K-mer
  2. Align AbySS contigs back to E.coli template using bowtie to assess mapping rate & coverage
  3. Filter the read to >300bp and BLAST to nt.PE alignment using Bowtie to assess chimerics