Hybrid error correction and de novo assembly of single-molecule sequencing reads——文獻學習
今天介紹的文獻是關於三代測序的拼接算法的研究，或者準確來講是一個利用二代測序和三代測序結果來拼接基因組序列的方法，當然這篇文章其實只是做了一個部分的創新，大部分拼接的原理是基於已有的拼接算法。當然，這篇文獻其實有點舊了，是2012年發表在nature子刊biotechnology上的。 標題裏的de novo是一個拉丁語貌似，文獻中比較喜歡用這個詞表示重新、從頭開始的意思。single-molec
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相關文章
- 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. 測序深度和覆蓋度（Sequencing depth and coverage）