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Hi,
Thanks for developing this. I had a question about the output files and, after reading the README, I am still unsure on the expected output.
I am using PE150 MiSeq reads. Performed a SPAdes assembly (this output is *.scaffolds.fasta). These genomes are highly fragmented but >99% ANI to a reference genome that I have previously sequenced fully with PACBIO (complete genome; 3.77Mb). However, when I use AlignGraph, the output files confuse me.
One example:
Sequence_ID Total_Contigs Genome_length Largest_Contig n50 GC_Percent
Desert-2-3.extended 16 3335782 1108581 343422 70
Desert-2-3.remain 19 707214 201094 182646 71
Desert-2-3.scaffolds 73 3740981 508547 119510 71
This appears to me that I would need to concatenate the *extended.fasta with the *remaining.fasta file to get the desired genome? Any clarification would be great.
Here is the command I am using:
AlignGraph --read1 $OUTDIR/${mate}_R1_001.fasta --read2 $OUTDIR/${mate}_R2_001.fasta \
--fastMap --contig $genome.scaffolds.fasta --genome $REFGENOME \
--distanceLow 550 --distanceHigh 1550 \
--extendedContig $genome.extended.fa --remainingContig $genome.remain.fa
Thank you!
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