Automated Author ProfileZhang, Wanchang
0000-0003-1040-2516
Zhang, Wanchang
Current S-Index
Sum of Dataset Indices for all datasets
Average Dataset Index per Dataset
Average Dataset Index per dataset
Total Datasets
Total datasets for this author
Average FAIR Score
Average FAIR Score per dataset
Total Citations
Total citations to the author's datasets
Total Mentions
Total mentions of the author's datasets
S-Index Interpretation
The S-Index (Sharing Index) is a comprehensive metric that represents the cumulative impact of all your datasets. It is calculated as the sum of Dataset Index scores across all your claimed datasets.
What it means:
- A higher S-index indicates greater overall impact of your datasets relative to typical datasets in their fields of research
- The S-Index grows as you add more datasets or as existing datasets gain more citations and mentions
- It provides a single number to track your research data impact over time
Current S-Index: 11.0 (sum of 15 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
Resequencing data of Betta siamorientalis and stiktos
Authors
- Zhang, Wanchang
Resequencing data of Betta siamorientalis and stiktos
Authors
- Zhang, Wanchang
We have built a full-sib F1 family consisting 200 individuals of the yellow drum. We sequenced the whole genomes of the parents and the F1 offspring applying Illumina HiSeq X TEN platform. The raw reads were filtered by removing low quality reads and adapters by using Trimmomatic (v0.36) 41. An average of 9.8 Gb data was obtained for each individual. The clean reads were mapped to the reference assembly using “BWA-MEM” in BWA (v0.7.10-r78) 42. Genomic alignments showed that the average sequence depth of the parents and the F1 individuals was 45.9× and 15.54×, respectively.For SNP calling, the high-quality mapped reads of the 202 individuals were analyzed in GATK (v 3.3-0) 43. A number of 3.36 million raw SNPs were called for subsequent filtering: 1) only bi-allele SNPs were retained in all individuals. 2) genotype depth of SNPs of parents and offspring were between 10-30 and 5-20, respectively. 3) genotype quality of all variants > 10. 4) all SNPs in the parents should not be missing and at least one of the parents should be heterozygous. 5) missing rate of each SNP should be < 15%. Then filtered SNPs were obtained and transmitted into JoinMap4.1 44 for Chi-squared test (P <0.05). Finally, 6,219 SNPs were used for constructing linkage map by Joinmap4.1. Twenty-four linkage groups were clustered using 6,219 SNP markers across the yellow drum genome, with the number of SNPs on each chromosome ranging from 179 to 359. Each linkage group contained an average of 260 SNP markers. The maximum likelihood method was used to sort the markers on each linkage group and estimate the genetic distances between markers. The consensus map spanned 4,300.2 cM and covered nearly the whole genome with a resolution of 0.69 cM. Compared to the previous linkage map constructed by Qiu et al. 5, we have used more individuals with more genetic markers and produced a genetic linkage map with higher resolution. This high-density linkage map will facilitate the ongoing marker-assisted selection and genomic study of the yellow drum.
Authors
- Dongdong Wu ;
- Zhang, Wanchang
Detailed sequencing statistics and phenotypes of 202 individuals in this project.
Authors
- Dongdong Xu ;
- Zhang, Wanchang
Detailed sequencing statistics and phenotypes of 202 individuals in this project.
Authors
- Dongdong Xu ;
- Zhang, Wanchang
This table gives a list of TE types and frequencies in the Yellow drum genome.
Authors
- Dongdong Xu ;
- Zhang, Wanchang
This table gives a list of TE types and frequencies in the Yellow drum genome.
Authors
- Dongdong Xu ;
- Zhang, Wanchang
We provide orignal outputs of the phylogenic tree, divergence time, expanded and contracted gene families, synteny analysis of the Yellow drum and other 11 bony fish species.
Authors
- Dongdong Xu ;
- Zhang, Wanchang
We provide orignal outputs of the phylogenic tree, divergence time, expanded and contracted gene families, synteny analysis of the Yellow drum and other 11 bony fish species.
Authors
- Dongdong Xu ;
- Zhang, Wanchang
We have built a full-sib F1 family consisting 200 individuals of the yellow drum. We sequenced the whole genomes of the parents and the F1 offspring applying Illumina HiSeq X TEN platform. The raw reads were filtered by removing low quality reads and adapters by using Trimmomatic (v0.36) 41. An average of 9.8 Gb data was obtained for each individual. The clean reads were mapped to the reference assembly using “BWA-MEM” in BWA (v0.7.10-r78) 42. Genomic alignments showed that the average sequence depth of the parents and the F1 individuals was 45.9× and 15.54×, respectively.For SNP calling, the high-quality mapped reads of the 202 individuals were analyzed in GATK (v 3.3-0) 43. A number of 3.36 million raw SNPs were called for subsequent filtering: 1) only bi-allele SNPs were retained in all individuals. 2) genotype depth of SNPs of parents and offspring were between 10-30 and 5-20, respectively. 3) genotype quality of all variants > 10. 4) all SNPs in the parents should not be missing and at least one of the parents should be heterozygous. 5) missing rate of each SNP should be < 15%. Then filtered SNPs were obtained and transmitted into JoinMap4.1 44 for Chi-squared test (P <0.05). Finally, 6,219 SNPs were used for constructing linkage map by Joinmap4.1. Twenty-four linkage groups were clustered using 6,219 SNP markers across the yellow drum genome, with the number of SNPs on each chromosome ranging from 179 to 359. Each linkage group contained an average of 260 SNP markers. The maximum likelihood method was used to sort the markers on each linkage group and estimate the genetic distances between markers. The consensus map spanned 4,300.2 cM and covered nearly the whole genome with a resolution of 0.69 cM. Compared to the previous linkage map constructed by Qiu et al. 5, we have used more individuals with more genetic markers and produced a genetic linkage map with higher resolution. This high-density linkage map will facilitate the ongoing marker-assisted selection and genomic study of the yellow drum.
Authors
- Dongdong Wu ;
- Zhang, Wanchang