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FastqReader Error? #1

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@Atalasia

I am trying to run RNA-Bloom for Nanopore cDNA sequencing reads, but it seems like it is failing....

Below is the message I am getting if I run the program with an input fastq (uncompressed) file.

ERROR: Unsupported file format detected in input file `sample.fastq`. Only FASTA and FASTQ formats are supported.
rnabloom.io.FileFormatException: Unsupported file format detected in input file `sample.fastq`. Only FASTA and FASTQ formats are supported.
        at rnabloom.RNABloom.checkInputFileFormat(RNABloom.java:309)
        at rnabloom.RNABloom.main(RNABloom.java:4750)

Below is the message I am getting if I run the program with an input bgzip compressed fastq file. It runs for some time and then it dies. There's bunch of intermediary files.

...
Parsed 4,308,866 sequences.
        Corrected: 4,308,203(99.98461%)
        Discarded: 663(0.015386879%)
Reads corrected in 54m 50s
Clustering long reads for "rnabloom"
ERROR: null
java.lang.NullPointerException
        at rnabloom.io.FastaReader.<init>(FastaReader.java:44)
        at rnabloom.RNABloom.clusterLongReads(RNABloom.java:2210)
        at rnabloom.RNABloom.clusterLongReads(RNABloom.java:3740)
        at rnabloom.RNABloom.main(RNABloom.java:5150)

Below are the args :
args: [-ntcard, -c, 3, -k, 17, -indel, 10, -e, 3, -p, 0.8, -long, sample.fastq, -t, 16, -outdir, .]

Below is the java version :

java version "11.0.2" 2019-01-15 LTS
Java(TM) SE Runtime Environment 18.9 (build 11.0.2+9-LTS)
Java HotSpot(TM) 64-Bit Server VM 18.9 (build 11.0.2+9-LTS, mixed mode)

I've tried with different cDNA samples (all Nanopore) but they all give the same error.

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