Automated Author Profile

Zhang, Wanchang

0000-0003-1040-2516

Current S-Index

11.0

Sum of Dataset Indices for all datasets

Average Dataset Index per Dataset

0.7

Average Dataset Index per dataset

Total Datasets

15

Total datasets for this author

Average FAIR Score

64.5%

Average FAIR Score per dataset

Total Citations

5

Total citations to the author's datasets

Total Mentions

0

Total mentions of the author's datasets

S-Index Interpretation

S-Index Over Time

Cumulative Citations Over Time

Cumulative Mentions Over Time

Datasets

Resequencing data of Betta siamorientalis

Resequencing data of Betta siamorientalis and stiktos

Authors

  • Zhang, Wanchang
0 Citations0 Mentions85% FAIR0.3 Dataset Index
10.6084/m9.figshare.152456132021

Resequencing data of Betta siamorientalis

Resequencing data of Betta siamorientalis and stiktos

Authors

  • Zhang, Wanchang
0 Citations0 Mentions85% FAIR0.3 Dataset Index
10.6084/m9.figshare.15245613.v12021

High-density genetic map of the yellow drum (Nibea albiflora)

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
0 Citations0 Mentions85% FAIR0.1 Dataset Index
10.6084/m9.figshare.12250910.v12020

Phenotypic descriptives of 202 yellow drum individuals

Detailed sequencing statistics and phenotypes of 202 individuals in this project.

Authors

  • Dongdong Xu ;
  • Zhang, Wanchang
0 Citations0 Mentions15% FAIR0.4 Dataset Index
10.6084/m9.figshare.12317489.v12020

Phenotypic descriptive of 202 yellow drum individuals

Detailed sequencing statistics and phenotypes of 202 individuals in this project.

Authors

  • Dongdong Xu ;
  • Zhang, Wanchang
0 Citations0 Mentions85% FAIR0.3 Dataset Index
10.6084/m9.figshare.12317489.v22020

List of TE types and frequencies in the yellow drum

This table gives a list of TE types and frequencies in the Yellow drum genome.

Authors

  • Dongdong Xu ;
  • Zhang, Wanchang
0 Citations0 Mentions48% FAIR1.2 Dataset Index
10.6084/m9.figshare.126649102020

List of TE types and frequencies in the yellow drum

This table gives a list of TE types and frequencies in the Yellow drum genome.

Authors

  • Dongdong Xu ;
  • Zhang, Wanchang
0 Citations0 Mentions56% FAIR1.4 Dataset Index
10.6084/m9.figshare.12664910.v12020

Comparative genomic analyses of the Yellow drum

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
1 Citation0 Mentions85% FAIR2.5 Dataset Index
10.6084/m9.figshare.122096722020

Comparative genomic analyses of the Yellow drum

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
0 Citations0 Mentions56% FAIR1.4 Dataset Index
10.6084/m9.figshare.12209672.v12020

High-density genetic map of the yellow drum (Nibea albiflora)

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
1 Citation0 Mentions85% FAIR0.7 Dataset Index
10.6084/m9.figshare.122509102020