Specifying coordinates in TOML

[looselab]

Specifying coordinates in TOML

[kevbrick]

Thanks @alexomics. Very helpful. Just ~1,000 reads were sequenced without being unblocked; that's close to what I'd expect for 1.5% of the genome. I minimapped these reads to the genome and saw about 4x enrichment on chr12, so looks like it worked fine! I'll run a bigger test later today to verify ....

[mattloose]

Hi - can you post your toml file here so we can have a look?

[alexomics]

Could you give an example of the format that your targets are in? For entire contigs/chromosomes you can specify just the target name; for targets with coordinates you need to specify as contig,start,stop,strand. See the target formats in of TOML.md.

There is also a validator script that will let you know if your targets are recognised.

[kevbrick]

Hi Matt, Sorry for posting that prematurely. TOML is as follows: The validate script tells me all is OK.
[caller_settings]
config_name = "dna_r9.4.1_450bps_fast"
host = "127.0.0.1"
port = 5556

[conditions]
reference = "/home/kevbrick/genomes/hg38/Minimap2Index/genome.mmi"

[conditions.0]
name = "select_chr_12_start"
control = false
min_chunks = 0
max_chunks = 12
targets = ["chr12,1,50000000,+","chr12,1,50000000,-"]
single_on = "stop_receiving"
multi_on = "stop_receiving"
single_off = "unblock"
multi_off = "unblock"
no_seq = "proceed"
no_map = "proceed"

[alexomics]

What is the output from ru_validate?

[kevbrick]

ru_validate output:

😻 Looking good!
Generating experiment description - please be patient!
This experiment has 1 region on the flowcell

Using reference: /home/kevbrick/genomes/hg38/Minimap2Index/genome.mmi

Region 'select_chr_12_start' (control=False) has 1 target of which 1
are in the reference. Reads will be unblocked when classed as
single_off or multi_off; sequenced when classed as single_on or
multi_on; and polled for more data when classed as no_map or no_seq.

[mattloose]

I see @alexomics is on - I'll let him take this one!

But can you confirm - are you running with our bulk file here?

[kevbrick]

OK, great. Yep. I'm running with your bulk fast5 file.

[alexomics]

You are attempting to select 1.5% of the genome. How long are you running this test for? Are you seeing all reads being unblocked; are some reads being sequenced (no unblock sent)?

[kevbrick]

Yeah. I realise that a better test case would be to specify more of the genome. I ran this for ~2hr and get about 93,000 reads. How do I check if the reads are being unblocked / sequenced?

[alexomics]

There are a couple of log files that you can check. The first is the chunk_log.log (unless changed) and will be in the same directory read until was run from. You can run the following command to see how many of each mode was seen throughout the run. You are looking for single_on or multi_on which are the modes for when reads matched your range.

cut -f8 chunk_log.log | sort | uniq -c

Or in the run output directory (generated by MinKNOW) there will be a file called unblocked_read_ids.txt this is where all the read ids that read until sent are logged. You can search for all read ids that are in the sequencing summary that an unblock signal was not sent for:

grep -vFf unblocked_read_ids.txt sequencing_summary.txt

This last command might be very intensive/take a long time depending on the size of the sequencing summary or the unblocked read ids files.

[github-actions]

This issue is stale because it has been open 30 days with no activity. Remove stale label or comment or this will be closed in 5 days.

[github-actions]

This issue was closed because there has been no response for 5 days after becoming stale.