Strange results

Hello,

Thanks for this amazing tool. I am using fastv in perhaps an unusual way. I'm looking to detect the presence or absence of homologous gene clusters in metagenomic data. I started with ~17 million ORFs from our contigs, and clustered (mmseqs2, 95% identity) them into almost 4 million clusters. I want to detecte the clusters by detecting one or more unique kmers from their representative sequences.

I used unique_kmer (initially) to identify unique 24mers, but this took a long time, generated millions of files and unique 24-mers could not be found for a majority of sequences. I fell back on jellyfish, 32mers, and a convoluted pipeline of aligning the kmers against the cluster representatives and then filtering the sorted SAM file to include only non-overlapping kmers. This way the vast majority of cluster representatives had one or more unique kmers (mean of 3 and up to hundreds).

I applied fastv with minimal filtering and lowest thresholds (-A -G -Q -L -p 0.001 -d 0.001), but only ~100k of ~3.4 million cluster representatives are ever identified across all >200 samples.

I tested further by extracting only unique kmers from one sample and testing them against the sample reads: no hits!

Yet, when I search with seqkit, I find that the sequence file does indeed contain this kmer three times: "ATGAAATTCCATGGAATGGAATGGAATGGAAA"

e.g.
@K00150:405:HGVM5BBXY:6:2119:16741:38381/1
ATGAAATTCCATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGA*ATGAAATTCCATGGAATGGAATGGAATGGAAA*AGAATGGAATGGAATGAAATTCCATGGAATGGAATGGAATGGAATGGAATGAAATTCC
+
AAAFFJJJJJFAJJJJFJAFAAFJJFAFFJJAJJFF-FJAJ<JFJFJFFJFJJJFFAJJJFFJJJJJJJJFFJFFAAFJJFAFJFA-FJJFFJJJJFFFJFFJJJJFJFJJFJJJJFJJJF7FJFFFJJJF7FJJAAAFJF7AFJJFFAF

Can you advise why fastv seems not to be detecting it?

Thanks!

Just to add as a test case, I have provided a fastq sequence file with three reads

@K00150:405:HGVM5BBXY:6:2119:16741:38381/1
ATGAAATTCCATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGAAATTCCATGGAATGGAATGGAATGGAAAAGAATGGAATGGAATGAAATTCCATGGAATGGAATGGAATGGAATGGAATGAAATTCC
+
AAAFFJJJJJFAJJJJFJAFAAFJJFAFFJJAJJFF-FJAJ<JFJFJFFJFJJJFFAJJJFFJJJJJJJJFFJFFAAFJJFAFJFA-FJJFFJJJJFFFJFFJJJJFJFJJFJJJJFJJJF7FJFFFJJJF7FJJAAAFJF7AFJJFFAF
@K00150:414:HK5NLBBXY:1:1121:16457:6976/1
AATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGAAATTCCATGGAATGGAATGGAATGGAAAAGAATGGAATGGAATGAAATTCCATGGAATGGAATGGAATGGAATGGAATGAAATTCCATGGAATGGAATGG
+
AAFFFJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJFJJJJJFJJJJJJJJFJJJJJAFJJJFFF7<AJJJJFJFJJFJJJJJJJJJJJJJFJJFJJJJJFFFFAJFJJJJJJFJFFJJJF7---77AF<JFJJ-7-
@K00150:414:HK5NLBBXY:2:2212:24393:37396/1
AATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGGAATGAAATTCCATGGAATGGAATGGAATGGAAAAGAATGGAATGGAATGAAATTCCATGGAATGGAATGGAATGGAATGGAATGAAATTCCACGGAATGGAATGG
+
AAFFFJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJFJJJJJJJFJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJFJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJJFJJ

And a kmer database of:

>test
ATGAAATTCCATGGAATGGAATGGAATGGAAA

or

>test
ATGAAATTCCATGGAATGGAA

Neither the 21-mer or 32-mer was found in the sequences despite their presence.

21-mer example:

{
        "kmer_collection_scan_result": {

        },
        "summary": {
                "before_filtering": {
                        "total_reads":3,
                        "total_bases":450,
                        "q20_bases":443,
                        "q30_bases":432,
                        "q20_rate":0.984444,
                        "q30_rate":0.96,
                        "read1_mean_length":150,
                        "gc_content":0.373333
                },
                "after_filtering": {
                        "total_reads":3,
                        "total_bases":450,
                        "q20_bases":443,
                        "q30_bases":432,
                        "q20_rate":0.984444,
                        "q30_rate":0.96,
                        "read1_mean_length":150,
                        "gc_content":0.373333
                }
        },
        "filtering_result": {
                "passed_filter_reads": 3,
                "low_quality_reads": 0,
                "too_many_N_reads": 0,
                "too_short_reads": 0,
                "too_long_reads": 0
        },
        "duplication": {
                "rate": 0,
                "histogram": [2,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0],
                "mean_gc": [0.264706,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0]
        },
        "read1_before_filtering": {
                "total_reads": 3,
                "total_bases": 450,
                "q20_bases": 443,
                "q30_bases": 432,
                "total_cycles": 150,
                "quality_curves": {
                        ...                },
                "content_curves": {
                       ...
                }
        },
        "read1_after_filtering": {
                "total_reads": 3,
                "total_bases": 450,
                "q20_bases": 443,
                "q30_bases": 432,
                "total_cycles": 150,
                "quality_curves": {
                    ...
                },
                "content_curves": {
                     ....
                }
        },
        "command": "fastv -i tmp_test_targets.fastq -c tmp_test_kmers.fasta -A -G -V -Q -L -j tmp_test_fastv.json -h tmp_test_fastv.html -p 0.001 -d 0.001 "

I must misunderstand something important about how fastv is operating, or there is an error. I will be grateful for any advice.

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andrewjmc commented on Aug 18, 2021

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