When building contig maps, it seems as though GENESPACE is not finding gaps. I have confirmed that there are gaps for each contig in the .fasta file, but this does not translate when building the contig map.
This is the output of print(lapply(genomeGrs, head))
$gaps
GRanges object with 0 ranges and 0 metadata columns:
seqnames ranges strand
<Rle> <IRanges> <Rle>
-------
seqinfo: 26 sequences from an unspecified genome
$contigs
GRanges object with 6 ranges and 0 metadata columns:
seqnames ranges strand
<Rle> <IRanges> <Rle>
[1] scaffold_1 1-27316886 *
[2] scaffold_2 1-25469394 *
[3] scaffold_3 1-24508975 *
[4] scaffold_4 1-24030051 *
[5] scaffold_5 1-22507561 *
[6] scaffold_6 1-19840655 *
-------
seqinfo: 26 sequences from an unspecified genome
$telomeres
GRanges object with 6 ranges and 1 metadata column:
seqnames ranges strand | position
<Rle> <IRanges> <Rle> | <character>
[1] scaffold_1 4-14657 * | left
[2] scaffold_1 23850-24179 * | left
[3] scaffold_1 24687-25167 * | left
[4] scaffold_2 7-2262 * | left
[5] scaffold_2 2788-3025 * | left
[6] scaffold_2 25453885-25455888 * | right
-------
seqinfo: 26 sequences from an unspecified genome
When building contig maps, it seems as though GENESPACE is not finding gaps. I have confirmed that there are gaps for each contig in the .fasta file, but this does not translate when building the contig map.
This is the output of
print(lapply(genomeGrs, head))
Here is the script I'm using:
Please let me know if there are any additional files or snippets I can provide that might be helpful! Thank you!