Sequencing depth and breadth of the overall target region and 59 gene-specific regions. (XLSX 61 kb
23 candidate genes identified in the Chinese family with epilepsy, by whole-exome sequencing. (DOCX ...
Table S2. Recessive variants shared by a common gene in at least two different trios. Possibly patho...
Includes all 12 additional tables with every table on a separate spreadsheet. The file format is an ...
Information on known pathogenic or expected pathogenic variants according to the ACMG reportable gen...
Age and gender distributions in our cohort. All 421 subjects were under 18Â years old at the time of...
Titration of percentage target exome sequenced as a function of depth of sequencing thresholds. (XLS...
Additional file 2. Table S2. chILDRANZ gene panel (see PanelApp Australia Childhood Interstitial Lun...
Table S2. Shows all causative mutations identified in 72 patients from 68 families suffering from pr...
Supplementary methods the detailed description of the methods used for the molecular genetics analys...
Table S6. Information on all large >â 5-Mb homozygous regions per patient, detected in the exome....
Supplementary Materials and Tables. (a) The process of whole-exome sequencing (WES) analysis. (b) Ta...
Basic genotyping information of 40 GWAÂ studies-derived SNPs in Chinese children. (XLSX 16 kb
Contains fulltext : 196384.pdf (publisher's version ) (Open Access)Currently, offe...
Association of 32 GWAÂ studies-derived SNP alleles with overweight in Chinese children. (XLSX 13 kb
Figure S2. Distribution of genes with novel mutations based on individual patients. (A) Distribution...
23 candidate genes identified in the Chinese family with epilepsy, by whole-exome sequencing. (DOCX ...
Table S2. Recessive variants shared by a common gene in at least two different trios. Possibly patho...
Includes all 12 additional tables with every table on a separate spreadsheet. The file format is an ...
Information on known pathogenic or expected pathogenic variants according to the ACMG reportable gen...
Age and gender distributions in our cohort. All 421 subjects were under 18Â years old at the time of...
Titration of percentage target exome sequenced as a function of depth of sequencing thresholds. (XLS...
Additional file 2. Table S2. chILDRANZ gene panel (see PanelApp Australia Childhood Interstitial Lun...
Table S2. Shows all causative mutations identified in 72 patients from 68 families suffering from pr...
Supplementary methods the detailed description of the methods used for the molecular genetics analys...
Table S6. Information on all large >â 5-Mb homozygous regions per patient, detected in the exome....
Supplementary Materials and Tables. (a) The process of whole-exome sequencing (WES) analysis. (b) Ta...
Basic genotyping information of 40 GWAÂ studies-derived SNPs in Chinese children. (XLSX 16 kb
Contains fulltext : 196384.pdf (publisher's version ) (Open Access)Currently, offe...
Association of 32 GWAÂ studies-derived SNP alleles with overweight in Chinese children. (XLSX 13 kb
Figure S2. Distribution of genes with novel mutations based on individual patients. (A) Distribution...
23 candidate genes identified in the Chinese family with epilepsy, by whole-exome sequencing. (DOCX ...
Table S2. Recessive variants shared by a common gene in at least two different trios. Possibly patho...
Includes all 12 additional tables with every table on a separate spreadsheet. The file format is an ...
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