Feature Counts - potential bug with outfile.jcounts
1
0
Entering edit mode
@b9ada64c
Last seen 4 hours ago
Australia

Greetings to those familiar with Feature Counts,

We have one RNA sequencing, paired-end, 150bp file for which we estimate gene and junction counts using Feature Counts. We run Feature Counts in Linux.

Feature Counts version: 2.0.8 Feature Counts code:

$FCOUNTS -a GCF_000001405.40_GRCh38.p14_genomic.gtf -G GCF_000001405.40_GRCh38.p14_genomic.fna  -T 8 -J -M -s 0 -p --countReadPairs --largestOverlap -o outfile infile.bam

We have documented the following instance in a junction counts output file (outfile.jcounts) :

Genes:

PNKD TMBIM1

Situation (see attached picture in IGV):

PNKD gene overlaps TMBIM1 gene, and all transcripts. All TMBIM1 transcripts are in the PNKD intron. All TMBIM1 junction reads ~1000 are splitting between PNKD and TMBIM1 for multiple intron junctions. In outfile.jcounts PNKD is the primary gene, however has no exons located in this region. When we remove the PNKD gene from the GTF and recount with Feature Counts, the reads are assigned perfectly to TMBIM1, as the primary gene with NA as secondary gene, as it should. A check of gene counts using exon as feature correctly assigns counts to genes. This appears to be only a junction counting issue. The .gtf and .fna are Refseq 1405.40 files (as noted above) and are untouched. We use this as a simple verification of raw junction counts before analysing PSI. As you will also note, the reverse is also true with PNKD exon-exon junctions sharing read counts with a partially overlapped gene CATIP-AS2. We have encountered others and believe this may be a widespread event.

Here is the outfile.jcounts of that region:

PNKD    NA  NC_000002.12    218270602   +   NC_000002.12    218271381   +   17
PNKD    NA  NC_000002.12    218270602   +   NC_000002.12    218271424   +   4
PNKD    NA  NC_000002.12    218271549   +   NC_000002.12    218272570   +   14
PNKD    TMBIM1  NC_000002.12    218275621   -   NC_000002.12    218276026   -   74
PNKD    TMBIM1  NC_000002.12    218276079   -   NC_000002.12    218277004   -   46
PNKD    TMBIM1  NC_000002.12    218277099   -   NC_000002.12    218277366   -   90
PNKD    TMBIM1  NC_000002.12    218277453   -   NC_000002.12    218277633   -   96
PNKD    TMBIM1  NC_000002.12    218277670   -   NC_000002.12    218277935   -   73
PNKD    TMBIM1  NC_000002.12    218277974   -   NC_000002.12    218278515   -   123
PNKD    TMBIM1  NC_000002.12    218277992   -   NC_000002.12    218278515   -   1
PNKD    TMBIM1  NC_000002.12    218278118   -   NC_000002.12    218278515   -   2
PNKD    TMBIM1  NC_000002.12    218278565   -   NC_000002.12    218279038   -   128
PNKD    TMBIM1  NC_000002.12    218279091   -   NC_000002.12    218279289   -   101
PNKD    TMBIM1  NC_000002.12    218279091   -   NC_000002.12    218280026   -   6
PNKD    TMBIM1  NC_000002.12    218279353   -   NC_000002.12    218280026   -   109
PNKD    TMBIM1,MIR6513  NC_000002.12    218280126   -   NC_000002.12    218281940   -   26
PNKD    TMBIM1,MIR6513  NC_000002.12    218280126   NA  NC_000002.12    218292466   NA  34
PNKD    TMBIM1  NC_000002.12    218282181   -   NC_000002.12    218284039   -   1
PNKD    TMBIM1  NC_000002.12    218282181   -   NC_000002.12    218285763   -   1
PNKD    TMBIM1  NC_000002.12    218282181   -   NC_000002.12    218287207   -   1
PNKD    TMBIM1  NC_000002.12    218282181   NA  NC_000002.12    218292466   NA  71
PNKD    LOC105373881    NC_000002.12    218316364   +   NC_000002.12    218385147   +   3
PNKD    LOC105373880,LOC105373881   NC_000002.12    218316883   +   NC_000002.12    218317955   +   2
PNKD    CATIP-AS2   NC_000002.12    218323428   NA  NC_000002.12    218341591   NA  5
PNKD    CATIP-AS2   NC_000002.12    218323431   +   NC_000002.12    218339783   +   52
PNKD    CATIP-AS2   NC_000002.12    218339898   +   NC_000002.12    218340029   +   27
PNKD    CATIP-AS2   NC_000002.12    218340141   +   NC_000002.12    218340728   +   8
PNKD    CATIP-AS2   NC_000002.12    218340786   +   NC_000002.12    218341534   +   5
PNKD    CATIP-AS2   NC_000002.12    218341626   +   NC_000002.12    218341981   +   12
PNKD    CATIP-AS2   NC_000002.12    218342144   +   NC_000002.12    218343500   +   12
PNKD    CATIP-AS2   NC_000002.12    218343586   +   NC_000002.12    218344455   +   15
PNKD    CATIP-AS2   NC_000002.12    218344570   +   NC_000002.12    218344808   +   28

Has anyone encountered this before and know where things have gone wrong? Prof Smyth suggested we post here instead of Biostars, to hear some constructive feedback from the Subread authors.

Thanks in advance, Chris. PNKD_TMBIM1 PNKD_TMBIM1_closeup
featurecounts Rsubread • 212 views
ADD COMMENT •
0
Entering edit mode

When you use featureCounts to count junctions with the -J option, it doesn't check if the junction is exactly overlap with exons of genes. Instead, it looks at the whole gene regions (from the first base to the last base of each gene). If the junction is anywhere within the region of a gene, it's assigned to that gene.

ADD REPLY •
0
Entering edit mode

Hi Yang Liao, thanks for the note.

We use Feature Counts extensively for gene-level counting (exon features).

Unfortunately though, and I'll wait for other people's professional opinion to comment on this further, from your comments I disagree with the definition of the function and how it works.

I feel users should not have to go and check whether the splice junctions indeed exist in every primary gene of the list (now that I know it is not tracking junction counts as per the annotation).

Further, there are possibly 15 000 occurrences of this, in this one bam file aligned to Refseq 1405.40 . Gencode has similar overlapped genes on the same strand and opposite strand.

Also in the example provided, the junction data rows correctly annotate the strand and coordinates of TMBIM1 (strand negative) in site 1 and site 2, not PNKD (strand positive). The only column recording any information relating to PNKD is the primary gene column.

Other programs annotate and count the splices correctly using 2 exons and corresponding transcript IDs, and the transcript IDs' corresponding Gene Id's to build the junction correctly. (Never using the gene start and end coordinate to act as a bucket for any junctions located in the region).

While it was extremely convenient and useful to use -J and obtain junction counts at the same time as our gene counts, now that I know it is incorrect and I will no longer be able to this feature. We almost submitted this data to external reviewers and it would have been incorrect. However, we counted the junctions with several programs and documented the discrepancy.

Having said of all the above, we hope the moderators agree there is an error here that should be addressed because having this feature in FeatureCounts is extremely useful.

Thanks for considering, Chris.

ADD REPLY •
0
Entering edit mode
@gordon-smyth
Last seen 1 hour ago
WEHI, Melbourne, Australia

The behavior that you have documented is expected and is explained in the featureCounts documentation.

The first thing to understand is that featureCounts detects junction reads de novo, without reference to the GTF annotation. This is a very powerful facility, because it allows featureCounts to find novel exon-exon junctions that are not annotated. Experience shows that novel transcript and junctions that are not in any GTF file are empirically very common in RNA-seq data. However, annotating novel junctions is not straightforward and doing that comprehensively is somewhat beyond the current scope of featureCounts.

In general, featureCounts has no way of knowing for sure which gene an exon-exon junction belongs to. The junction might be novel and it might originate from exons or transcripts that are not in the GTF file. So featureCounts currently takes the very simple approach of listing all the possible genes that the junction might potentially belong to. Specifically, it lists all the genes for which the junction falls within the genomic region, from TSS to TES, of that gene.

Each junction consists of two genomic positions ("splice sites"). If there is only one gene containing both splice sites, then that gene is specified as the "Primary Gene" and all other candidates are listed as "Secondary Genes". If there is only one gene containing containing either of the two splice sites then, again, that gene is specified as the "Primary Gene" and all other candidates are lists as "Secondary Genes". If there are two or more genes that contain both splice sites, then featureCounts makes an arbitrary choice -- it chooses the candidate gene with the first occuring genomic region to be the "Primary Gene". This behaviour is explained pretty clearly in the documentation, which says:

When the primary and secondary genes overlap same number of splice sites, the gene with the smallest leftmost base position is selected as the primary gene.

Now you may say, featureCounts could check whether the detected junction matches one of the annotated exon-exon junctions in the GTF file, because that might resolve which candidate gene is the correct Primary Gene, and I would agree with you. I am been thinking about this for a couple of years, but it is not as straightforward as you might think. What if the junction is just one base different from an annotated junction? Is that acceptable variation? Perhaps we might associate the junction with the annotated junction, on the same strand, that it is closest to? But such as strategy is far from foolproof and involves more programming. So, for the time being, featureCounts is taking a simple and sometimes arbitrary choice that nevertheless clearly documented.

The behavior is not a bug or an error, because the software behaves as documented.
ADD COMMENT •
0
Entering edit mode

Hi Gordon,

Thank you for pointing out that FeatureCounts detects junction reads de novo. It is not in the manual, and maybe could be. Given your statement, now I understand the behaviour we observe, though not sure of the thoughts behind it.

Probably the most productive point to raise is that for -J, it should be adamantly stated it is de novo, and does not look into the gtf for any overlapping gene domains until printing the output file. It would be useful if the strand is correct for the primary and secondary gene (e.g as noted above, PNKD and TMBIM1 are both recorded as negative strand in the Site 1 and Site 2 output. However PNKD is positive strand.)

The manual's note on Primary and secondary gene candidate selection made sense to us and was not the issue. The issue was these junctions align with known annotated splices. As per QORTS, MAJIQ etc it seems to be straightforward for software to keep track of known vs unknown splices. With the programs noted, the output is recorded for both de novo and annotated junctions (e.g 2 default output files: QC.spliceJunctionCounts.knownSplices.txt.gz, QC.spliceJunctionCounts.novelSplices.txt.gz). The junctions are annotated as known TMBIM1 junctions in this file.

And we too, find novel exon-exon junctions to be a powerful research prospect. But at this stage in the project annotated splices with a high degree of research evidence take precedence.

I would have liked the reason to have been that it got missed, because your accuracy on exon level feature counting ( meta gene ) is so accurate in relation to ambiguity. It is fantastic for finding RNA count associated noise.

We wanted to combine feature counts junctions with our already existing gene counts summarization prior to splicing detection. We will not be able to do that with any accuracy in relation to the splice being correctly identified, first as annotated or finally, as de novo.

So, we will avoid -J in future, and use a more correct counting tool in future for annotated junction counting, and to document any novel splices, if research and depth of library can validate de novo splices in future.

Thanks for the explanation, Chris

ADD REPLY •
0
Entering edit mode

Hi Gordon,

Sorry, I didn't see the added response to your original answer.

I think that would be a great idea; a novel junction to annotated junction proximity output column. So if the novel junction read is n bases (set by the user) away from the annotated splice then report as "novel", but, with an annotation proximity value. And, the ability to collapse the counts into the annotated junction (another flag as set by the user).

Also, that would set it apart from other junction counting programs.

Regards, Chris

ADD REPLY •
0
Entering edit mode

I agree that the current behavior is not fully satisfactory and, indeed, it has prevented me from using the junction read counts from featureCounts myself in my own investigations of alternative splicing. But we do what we can within the time available. featureCounts is a large program with a large number of options. It is maintained long term without any ongoing funding by a couple of hard working scientists who have many other calls on their time. There is a lack of funding in Australia for long term maintenance of research software.

Regarding novel junctions, the junction detection is actually done by the aligner rather than by featureCounts itself. We use featureCounts junction counting as a followup to the subjunc aligner, and the fact that subjunc is detecting junctions de novo is documented.

ADD REPLY •

Login before adding your answer.

Similar Posts
Loading Similar Posts
Traffic: 600 users visited in the last hour
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6