Open lskatz opened 4 years ago
And my question leading into this was whether the bam file is all reads mapped against the assembly or only those trimmed/cleaned/flash'd.
@lskatz can you look at the perl code and tell me? :)
The original (or trimmomaticked originals if --trim) are used for alignment/correction.
I do NOT use the FLASH ones because one of the potential errors I want to correct is mis-FLASH-ed reads.
I took some language from
Filename | Description |
---|---|
contigs.fa |
The final assembly you should use |
shovill.log |
Full log file for bug reporting |
shovill.corrections |
List of post-assembly corrections |
contigs.gfa |
Assembly graph (spades) |
contigs.fastg |
Assembly graph (megahit) |
contigs.LastGraph |
Assembly graph (velvet) |
skesa.fasta |
Raw assembly (skesa) |
spades.fasta |
Raw assembled contigs (spades) |
megahit.fasta |
Raw assembly (megahit) |
velvet.fasta |
Raw assembly (velvet) |
flash.extendedFrags.fastq.gz |
Single-end reads from Flash, ie, merged reads |
flash.hist |
Numeric histogram of merged read lengths. |
flash.histogram |
Visual histogram of merged read lengths. |
flash.notCombined_1.fastq.gz |
R1 reads not combined in Flash |
flash.notCombined_2.fastq.gz |
R2 reads not combined in Flash |
R1.cor.fq.gz |
Corrected R1 reads from Lighter |
R1.fq.gz |
Original R1 |
R1.sub.fq.gz |
Subsampled R1 using --depth |
R2.cor.fq.gz |
Corrected R2 reads from Ligher |
R2.fq.gz |
Original R2 |
R2.sub.fq.gz |
Subsampled R2 using --depth |
shovill.bam |
Alignment of corrected reads from Trimmomatic against the vanilla assembly (skesa, spades, or megahit). Reads have been sorted with Samtools and filtered with samclip (ie, nuanced alignments have been removed). |
shovill.bam.bai |
Index file for shovill.bam |
skesa.fasta.amb |
(bwa index) text file, to record appearance of N (or other non-ATGC) in the ref fasta. |
skesa.fasta.ann |
(bwa index) text file, to record ref sequences, name, length, etc. |
skesa.fasta.bwt |
(bwa index) binary, the Burrows-Wheeler transformed sequence. |
skesa.fasta.fai |
Samtools index file |
skesa.fasta.pac |
(bwa index) binary, packaged sequence (four base pairs encode one byte). |
skesa.fasta.sa |
(bwa index) binary, suffix array index. |
skesa.fasta.uncorrected |
Assembly before pilon correction |
Not all files are described when I used
--keepfiles
. Could there be documentation for them, even if it's not in the main documentation? The additional files are the files I had after a skesa run. I am adding onto your table.contigs.fa
shovill.log
shovill.corrections
contigs.gfa
contigs.fastg
contigs.LastGraph
skesa.fasta
spades.fasta
megahit.fasta
velvet.fasta
flash.extendedFrags.fastq.gz
flash.hist
flash.histogram
flash.notCombined_1.fastq.gz
flash.notCombined_2.fastq.gz
R1.cor.fq.gz
R1.fq.gz
R1.sub.fq.gz
--depth
R2.cor.fq.gz
R2.fq.gz
R2.sub.fq.gz
--depth
shovill.bam
samclip
(ie, nuanced alignments have been removed).shovill.bam.bai
shovill.bam
skesa.fasta.amb
skesa.fasta.ann
skesa.fasta.bwt
skesa.fasta.fai
skesa.fasta.pac
skesa.fasta.sa
skesa.fasta.uncorrected