Hybrid error correction and de novo assembly of single-molecule sequencing reads——文献学习
今天介绍的文献是关于三代测序的拼接算法的研究，或者准确来讲是一个利用二代测序和三代测序结果来拼接基因组序列的方法，当然这篇文章其实只是做了一个部分的创新，大部分拼接的原理是基于已有的拼接算法。当然，这篇文献其实有点旧了，是2012年发表在nature子刊biotechnology上的。 标题里的de novo是一个拉丁语貌似，文献中比较喜欢用这个词表示重新、从头开始的意思。single-molec
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相关文章
- 1. Efficient Hybrid De Novo Error Correction and Assembly for Long Reads
- 2. Hybrid Error Correction approach and DeNovo Assembly for MinIon Sequencing Long Reads
- 3. An Error Correction and DeNovo Assembly Approach for Nanopore Reads Using Short Reads
- 4. Nanopore sequencing and assembly of a human genome with ultra-long reads
- 5. Efficient and accurate whole genome assembly and methylome profiling of E. coli
- 6. Comparative Evaluation of Genome Assemblers from Long-Read Sequencing for Plants and Crops
- 7. A Benchmark Study on Error Assessment and Quality Control of CCS Reads Derived from the PacBio RS
- 8. Comparative assessment of long-read error correction software applied to Nanopore RNA-sequencing dat
- 9. Improving Illumina assemblies with Hi‐C and long reads: An example with the North African dromedary
- 10. 测序深度和覆盖度（Sequencing depth and coverage）