Upload your next generation sequencing data in fastq or fasta format. Files will be processed using the NTM-Profiler pipeline with default parameters. You may select the technology used to generate the data (Illumina or Oxford Nanopore). Samples will be process with a first in first out policy so please be patient as there may be runs waiting to be processed before yours.
Please note: at the moment we can only accomodate uploads of files under 4GB. If you have files which are larger or you require many isolates to be processed and have access to a linux or macOS operating system then it might be worthwhile to run the commandline version of NTM-Profiler. For more information on this please visit the github repository.

Please drop your files in here and click submit when done.

Platform:
Filetype:
File suffix:
Read suffix. Use this option to change the default suffix of files. For example if your fastq file is named sample1_R1.fastq.gz then your suffix should be _R1.fastq.gz
Forward file suffix:
Reverse file suffix:
File suffix:
Read suffix. Use this option to change the default suffix of files. For example if your fastq file is named sample1.fna then your suffix should be .fna
File suffix:
File suffix:
Read suffix. Use this option to change the default suffix of files. For example if your fastq file is named sample1.fna then your suffix should be .fna
File suffix: