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Figure 1 from RobiNA: a user-friendly, integrated software solution for RNA- Seq-based transcriptomics | Semantic Scholar
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Cancers | Free Full-Text | miRGalaxy: Galaxy-Based Framework for Interactive Analysis of microRNA and isomiR Sequencing Data
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SARS-CoV-2 Sequencing, Polygenic Risk Scores, and Precision Medicine: High-throughput Solutions - Sampled
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Frontiers | CNV-MEANN: A Neural Network and Mind Evolutionary Algorithm-Based Detection of Copy Number Variations From Next-Generation Sequencing Data
GitHub - broadinstitute/picard: A set of command line tools (in Java) for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF.
GitHub - samtools/samtools: Tools (written in C using htslib) for manipulating next-generation sequencing data
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Tools and Strategies for Long-Read Sequencing and De Novo Assembly of Plant Genomes: Trends in Plant Science
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FLEP-seq: simultaneous detection of RNA polymerase II position, splicing status, polyadenylation site and poly(A) tail length at genome-wide scale by single-molecule nascent RNA sequencing | Nature Protocols
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Extraction and Oxford Nanopore sequencing of genomic DNA from filamentous Actinobacteria - ScienceDirect
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Frontiers | An Optimized Tissue Dissociation Protocol for Single-Cell RNA Sequencing Analysis of Fresh and Cultured Human Skin Biopsies
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