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E.g. ftp://ftp-trace.ncbi.nlm.nih.gov/giab/ftp/data/AshkenazimTrio/HG002_NA24385_son/Ultralong_OxfordNanopore/
$ dsh-bio fastq-sequence-length -i combined_2018-05-18.fastq.gz | sort -n -r | head 322099 298433 283861 262525 247501
scala> val reads = sc.loadAlignments("combined_2018-05-18.fastq.gz") reads: org.bdgenomics.adam.rdd.read.AlignmentRecordRDD = ParquetUnboundAlignmentRecordRDD with 0 reference sequences, 0 read groups, and 0 processing steps scala> val lengths = reads.rdd.map(_.sequence.length()).collect() lengths: Array[Int] = Array(641, 3082, 10000, 10000, 10000, ... scala> lengths.sortBy(-1 * _).take(10) res3: Array[Int] = Array(10000, 10000, 10000, 10000, 10000, 10000, 10000, 10000, ...
The text was updated successfully, but these errors were encountered:
[ADAM-1992] Make maximum FASTQ read length configurable.
cf1204d
Resolves bigdatagenomics#1992.
2ca826e
No branches or pull requests
E.g. ftp://ftp-trace.ncbi.nlm.nih.gov/giab/ftp/data/AshkenazimTrio/HG002_NA24385_son/Ultralong_OxfordNanopore/
The text was updated successfully, but these errors were encountered: