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Description of the genomic datasets (nanopore and illumina).
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创建时间：
2018-11-05
相关数据集
Nanopore sequencing of cDNA amplicons mapped to their original genomic sequences.
Results of nanopore sequencing of cDNA amplicons mapped to their original genomic sequences. Sequences were mapped using "conform_introns.py" script from associated GitHub repository (based on Porecho
Figshare2024-07-26 更新70
Illumina sequencing plate1
This file contains both forward (t1-UNIS_S1_L001_R1_001.fastq) and reverse (t1-UNIS_S1_L001_R2_001.fastq) Illumina read data and associated barcode mapping files. In Mapfile_T1 forward primer is linke
DataONE2015-11-05 更新60
Supplementary Data - Nanopore cDNA With and Without mtDNA
Update (v1.5.6-countAnalysis): added / updated a script to convert transcript mappings to a count table: count_analysis.r Update (v1.5.5-Int): added intermediate (post-demultiplexing) demonstration da
Zenodo2020-07-30 更新30
Additional file 3 of Dynamic nanopore long-read sequencing analysis of HIV-1 splicing events during the early steps of infection
Additional file 3: Table S3. NL4-3 splice site counts in HIV-1 expressing samples. Reads overlapping potential SD/SA sites were counted and pooled for each HIV-1 expressing sample (infected T cells; T
DataCite Commons2020-08-25 更新60
Accuracy and running time on R9 data.
The results of base calling were aligned to the reference using BWA-MEM [28]. The first column reports the percentage of reads that aligned to the reference on at least 90% of their length. The accura
NIAID Data Ecosystem50
