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UnSplicer: mapping spliced RNA-seq reads in compact genomes and filtering noisy splicing
Accurate mapping of spliced RNA-Seq reads to genomic DNA has been known as a challenging problem. Despite significant efforts invested in developing efficient algorithms, with the human genome as a primary focus, the best solution is still not known. A recently introduced tool, TrueSight, has demons...
Tallennettuna:
| Päätekijät: | , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3936741/ https://ncbi.nlm.nih.gov/pubmed/24259430 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkt1141 |
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