Automated Author ProfileWeiss, Martina
Weiss, Martina
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: 10.1 (sum of 23 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
The table in CVS format contains raw morphometric measurements (49 traits) of females and males (80 individuals) belonging to four mitochondrial lineages of Echinogammarus sicilianus
Authors
- Hupalo, Kamil ;
- Copilas-Ciocianu, Denis ;
- Leese, Florian ;
- Weiss, Martina
The table in CVS format contains raw morphometric measurements (49 traits) of females and males (80 individuals) belonging to four mitochondrial lineages of Echinogammarus sicilianus
Authors
- Hupalo, Kamil ;
- Copilas-Ciocianu, Denis ;
- Leese, Florian ;
- Weiss, Martina
DNA barcode data hosted in the Data Portal of the Barcode of Life Data Systems. Records consist of specimen metadata, specimen images, and sequence data.
Authors
- Hupało, Kamil ;
- Copilas-Ciocianu, Denis ;
- Leese, Florian ;
- Weiss, Martina
No description available
Authors
- Weigand, Hannah ;
- Weiss, Martina ;
- Cai, Huimin ;
- Li, Yongping ;
- Zhang, Christine ;
- Leese, Florian
No description available
Authors
- Weigand, Hannah ;
- Weiss, Martina ;
- Cai, Huimin ;
- Li, Yongping ;
- Zhang, Christine ;
- Leese, Florian
No description available
Authors
- Weigand, Hannah ;
- Weiss, Martina ;
- Cai, Huimin ;
- Li, Yongping ;
- Zhang, Christine ;
- Leese, Florian
Pairwise Fst values (below diagonal) and corresponding p-values (above diagonal) calculated using13 microsatellites genotyped in 45 individuals.
Authors
- Vendrami, David L. J. ;
- Telesca, Luca ;
- Weigand, Hannah ;
- Weiss, Martina ;
- Fawcett, Katie ;
- Lehman, Katrin ;
- M. S. Clark ;
- Leese, Florian ;
- McMinn, Carrie ;
- Moore, Heather ;
- Hoffman, Joseph I.
Summary of the results obtained from different de novo assemblies of the ddRAD data generated using different values for three main parameters -m, -M and -n within the denovo_map.pl Script in Stacks. -m and -M define the minimum number of raw reads and the maximum number of mismatches between loci when creating a stack within the same individual respectively. -n corresponds to the number of mismatches allowed between loci when processing multiple individuals. For each tested combination of parameters, we report the total number of tags, the number of tags present in all of the individuals, observed heterozygosity, average depth of coverage, and the number of SNPs obtained after filtering.
Authors
- Vendrami, David L. J. ;
- Telesca, Luca ;
- Weigand, Hannah ;
- Weiss, Martina ;
- Fawcett, Katie ;
- Lehman, Katrin ;
- M. S. Clark ;
- Leese, Florian ;
- McMinn, Carrie ;
- Moore, Heather ;
- Hoffman, Joseph I.
Summary of the results obtained from different de novo assemblies of the ddRAD data generated using different values for three main parameters -m, -M and -n within the denovo_map.pl Script in Stacks. -m and -M define the minimum number of raw reads and the maximum number of mismatches between loci when creating a stack within the same individual respectively. -n corresponds to the number of mismatches allowed between loci when processing multiple individuals. For each tested combination of parameters, we report the total number of tags, the number of tags present in all of the individuals, observed heterozygosity, average depth of coverage, and the number of SNPs obtained after filtering.
Authors
- Vendrami, David L. J. ;
- Telesca, Luca ;
- Weigand, Hannah ;
- Weiss, Martina ;
- Fawcett, Katie ;
- Lehman, Katrin ;
- M. S. Clark ;
- Leese, Florian ;
- McMinn, Carrie ;
- Moore, Heather ;
- Hoffman, Joseph I.
Design of the P7 adapters used during the preparation of the ddRAD library.
Authors
- Vendrami, David L. J. ;
- Telesca, Luca ;
- Weigand, Hannah ;
- Weiss, Martina ;
- Fawcett, Katie ;
- Lehman, Katrin ;
- M. S. Clark ;
- Leese, Florian ;
- McMinn, Carrie ;
- Moore, Heather ;
- Hoffman, Joseph I.