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How can I use Bowtie to output aligned paired end fastq files as two separate fastq files ie. aligned_1.fastq and aligned_2.fastq. Right now I can only produce a single output file containing both aligned paired end reads.
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Performena is a digital-first creative agency based in the UAE. We craft resonant brand experiences through strategic consultancy, creative services, media planning, programmatic advertising, and custom technology solutions.
Our journey began with a vision to revolutionize digital marketing. We combine data-driven insights with creative storytelling to deliver impactful campaigns that drive measurable results. Our team of wild hearts and tech wizards work tirelessly to unlock your brand's...Today, 05:26 AM -
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
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The field of immunogenetics explores how genetic variations influence immune responses and susceptibility to disease. In a recent SEQanswers webinar, Oscar Rodriguez, Ph.D., Postdoctoral Researcher at the University of Louisville, and Ruben MartÃnez Barricarte, Ph.D., Assistant Professor of Medicine at Vanderbilt University, shared recent advancements in immunogenetics. This article discusses their research on genetic variation in antibody loci, antibody production processes,...11-06-2024, 07:24 PM