Dear all,
Im new to this world of seq'g. Right now i have a draft version of a genome (~300 mb) and some RNAseq runs of it from 454.
1. Which is the best software to align RNAseq ? I have us'd newbler and mira. Do you have any more suggestion?
2. How can I compare this both software (newbler and mira) ? To map back these RNA contigs to draft genome, which software I should use?
Your comments are greatly appreciated....
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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
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