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> This step should **not** be done if the data are RRBS (reduced representation bisulfite sequencing; see e.g., [bismark documentation](https://felixkrueger.github.io/Bismark/bismark/deduplication/)).
* sample-1_bismark_bt2_sorted*.bam (bismark bowtie2 alignment bam file sorted by chromosomal coordinates, output from [Step 4c](#4c-sort-alignment-files) above if data are RRBS, or deduplicated bam file from [step 6](#6b-sort-deduplicated-alignment-files) if data are not RRBS and the bam file was deduplicated (e.g., sample-1_bismark_bt2_sorted.deduplicated.bam from above))
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* sample-1_bismark_bt2_sorted*.bam (bismark bowtie2 alignment bam file sorted by chromosomal coordinates, output from [Step 4c](#4c-sort-alignment-files) above if data are RRBS, or deduplicated bam file from [step 6b](#6b-sort-deduplicated-alignment-files) if data are not RRBS and the bam file was deduplicated (e.g., sample-1_bismark_bt2_sorted.deduplicated.bam from above))
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* a directory holding the reference genome in fasta format (this pipeline version uses the Ensembl fasta file indicated in the `fasta` column of the [GL-DPPD-7110_annotations.csv](../../GeneLab_Reference_Annotations/Pipeline_GL-DPPD-7110_Versions/GL-DPPD-7110/GL-DPPD-7110_annotations.csv) GeneLab Annotations file))
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