Automated Author ProfileLack, Nathan
Lack, Nathan
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: 10.0 (sum of 10 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
Odd’s ratio and Fisher’s exact test p-values for a frequency difference between SNVs shared among all tumours and SNVs found private to tumours, with respect to dinucleotide context. The table includes results for Patients 1 and 2. Bold lines show significant results with odd’s ratio > 1. (XLS 20 kb)
Authors
- Acar, Ömer ;
- Özkurt, Ezgi ;
- Gulfem Demir ;
- Saraç, Hilal ;
- Alkan, Can ;
- Tarık Esen ;
- Somel, Mehmet ;
- Lack, Nathan
Odd’s ratio and Fisher’s exact test p-values for a frequency difference between SNVs shared among all tumours and SNVs shared among all samples, with respect to dinucleotide context and trinucleotide context. The table includes results for Patients 1 and 2. Bold lines show significant results with odd’s ratio > 1. (XLS 25 kb)
Authors
- Acar, Ömer ;
- Özkurt, Ezgi ;
- Gulfem Demir ;
- Saraç, Hilal ;
- Alkan, Can ;
- Tarık Esen ;
- Somel, Mehmet ;
- Lack, Nathan
Number of reads and number of detected SNVs and indels. Cov: coverage. The strict filtering criteria include the GATK quality score (“PASS”), excluding segmental duplications, removing SNVs included in dbSNPv.138, only including SNVs reliably genotyped in all 4 samples, and identified at least in 4 reads. See Material and Methods for details. (XLS 29 kb)
Authors
- Acar, Ömer ;
- Özkurt, Ezgi ;
- Gulfem Demir ;
- Saraç, Hilal ;
- Alkan, Can ;
- Tarık Esen ;
- Somel, Mehmet ;
- Lack, Nathan
Odd’s ratio and Fisher’s exact test p-values for a frequency difference between SNVs shared among all tumours and SNVs shared among all samples, with respect to dinucleotide context and resulting mutations. The table includes results for Patients 1 and 2. Bold lines show significant results with odd’s ratio > 1. (XLS 24 kb)
Authors
- Acar, Ömer ;
- Özkurt, Ezgi ;
- Gulfem Demir ;
- Saraç, Hilal ;
- Alkan, Can ;
- Tarık Esen ;
- Somel, Mehmet ;
- Lack, Nathan
Potential driver mutations in samples identified from COSMIC or ATLAS databases and literature. (XLS 33 kb)
Authors
- Acar, Ömer ;
- Özkurt, Ezgi ;
- Gulfem Demir ;
- Saraç, Hilal ;
- Alkan, Can ;
- Tarık Esen ;
- Somel, Mehmet ;
- Lack, Nathan
Potential driver mutations in samples identified from COSMIC or ATLAS databases and literature. (XLS 33 kb)
Authors
- Acar, Ömer ;
- Özkurt, Ezgi ;
- Gulfem Demir ;
- Saraç, Hilal ;
- Alkan, Can ;
- Tarık Esen ;
- Somel, Mehmet ;
- Lack, Nathan
Odd’s ratio and Fisher’s exact test p-values for a frequency difference between SNVs shared among all tumours and SNVs shared among all samples, with respect to dinucleotide context and resulting mutations. The table includes results for Patients 1 and 2. Bold lines show significant results with odd’s ratio > 1. (XLS 24 kb)
Authors
- Acar, Ömer ;
- Özkurt, Ezgi ;
- Gulfem Demir ;
- Saraç, Hilal ;
- Alkan, Can ;
- Tarık Esen ;
- Somel, Mehmet ;
- Lack, Nathan
Number of reads and number of detected SNVs and indels. Cov: coverage. The strict filtering criteria include the GATK quality score (“PASS”), excluding segmental duplications, removing SNVs included in dbSNPv.138, only including SNVs reliably genotyped in all 4 samples, and identified at least in 4 reads. See Material and Methods for details. (XLS 29 kb)
Authors
- Acar, Ömer ;
- Özkurt, Ezgi ;
- Gulfem Demir ;
- Saraç, Hilal ;
- Alkan, Can ;
- Tarık Esen ;
- Somel, Mehmet ;
- Lack, Nathan
Odd’s ratio and Fisher’s exact test p-values for a frequency difference between SNVs shared among all tumours and SNVs shared among all samples, with respect to dinucleotide context and trinucleotide context. The table includes results for Patients 1 and 2. Bold lines show significant results with odd’s ratio > 1. (XLS 25 kb)
Authors
- Acar, Ömer ;
- Özkurt, Ezgi ;
- Gulfem Demir ;
- Saraç, Hilal ;
- Alkan, Can ;
- Tarık Esen ;
- Somel, Mehmet ;
- Lack, Nathan
Odd’s ratio and Fisher’s exact test p-values for a frequency difference between SNVs shared among all tumours and SNVs found private to tumours, with respect to dinucleotide context. The table includes results for Patients 1 and 2. Bold lines show significant results with odd’s ratio > 1. (XLS 20 kb)
Authors
- Acar, Ömer ;
- Özkurt, Ezgi ;
- Gulfem Demir ;
- Saraç, Hilal ;
- Alkan, Can ;
- Tarık Esen ;
- Somel, Mehmet ;
- Lack, Nathan