筛选
科学数据
统计数据
共检索到190条 ,权限内显示50条;
Data from: Scrimer: designing primers from transcriptome data
- 负责人:
- DOI:
- doi:10.5061/dryad.2p4t3
- 摘要:
- peline called Scrimer that automates multiple steps, including adaptor removal, read mapping, selection of SNPs and multiple primer design from transcriptome data
Genomic data of the domestic goat (Capra hircus)
- 负责人:
- 关键词:
- Genomic
- DOI:
- doi:10.5524/100082
- 摘要:
- fragment maps derived from the whole genome mapping (WGM) technology developed by the Argus System (method described in this paper).Scaffolds derived from
Transcriptome sequencing of Capra hircus for different tissues.
- 负责人:
- BGI
- DOI:
- doi:10.26036/cnphis0000942
- 摘要:
- reference genome generated by combining Illumina short reads sequencing and a new automated and high throughput whole genome mapping system base
Data from: A dense linkage map of Lake Victoria cichlids improved the Pundamilia genome assembly and revealed a major QTL for sex-determination
- 负责人:
- 关键词:
- RAD;recombination rate;sex chromosome evolution;Cichlidae;XY system;amh;sex determination;synteny
- DOI:
- doi:10.5061/dryad.59q56g6
- 摘要:
- mapping. In the present study we identified and genotyped markers via restriction-site associated DNA (RAD) sequencing and constructed a genetic linkage map
Data from: Linkage mapping with paralogs exposes regions of residual tetrasomic inheritance in chum salmon (Oncorhynchus keta)
- 负责人:
- 关键词:
- tetrasomic inheritance;WGD;whole-genome duplication;Oncorhynchus keta;chum salmon;linkage mapping
- DOI:
- doi:10.5061/dryad.5b64r
- 摘要:
- Gene sequence similarity due to shared ancestry after a duplication event, that is paralogy, complicates the assessment of gene
Data from: Combining GWAS and RNA-seq approaches for detection of the causal mutation for hereditary junctional epidermolysis bullosa in sheep
- 负责人:
- 关键词:
- Junctional Epidermolysis Bullosa aplasia cutis congenita integrin beta-4 sheep association mapping whole skin transcriptomic analysis
- DOI:
- doi:10.5061/dryad.4j7jh
- 摘要:
- In this study, we demonstrate the use of a genome-wide association mapping together with RNA-seq in a reduced number of samples
Data from: Challenges and strategies in transcriptome assembly and differential gene expression quantification. A comprehensive in silico asse
- 负责人:
- DOI:
- doi:10.5061/dryad.3t3n7
- 摘要:
- ), technological processing (sequencing error ?, library normalization) and bioinformatic workflow (de novo vs. mapping assembly, reference genome quality) impact
Data from: Bioinformatic processing of RAD-seq data dramatically impacts downstream population genetic inference
- 负责人:
- DOI:
- doi:10.5061/dryad.q14c1
- 摘要:
- q data (>100 individuals) with 312 combinations of methodology (de novo vs. mapping to references of increasing divergence) and filtering criteria
Data from: Generative modeling of multi-mapping reads with mHi-C advances analysis of Hi-C studies
- 负责人:
- DOI:
- doi:10.5061/dryad.v7k3140
- 摘要:
- repetitive regions of genomes. We developed and validated mHi-C, a multi-read mapping strategy to probabilistically allocate Hi-C multi-reads. mHi-C exhibited
Data from: The mouse universal genotyping array: from substrains to subspecies
- 负责人:
- DOI:
- doi:10.5061/dryad.2p7ns
- 摘要:
- Genotyping microarrays are an important resource for genetic mapping, population genetics, and monitoring of the genetic integrity of laboratory