Code:
Error: At least one read sequence must be present in the project
in order to proceed with mapping or assembly.
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newblur help
I'm trying to run newblur with SCARF data converted to fastq using fq_all2std.pl but runAssembly keeps giving me an error after it indexes the fastq input.
I didn't think it required an sff file to run?
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Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.
Long-Read Sequencing
Long-read sequencing has seen remarkable advancements,...12-02-2024, 01:49 PM