Figure S1. Exonic Variant Read Distribution. The distribution of all exonic variant reads across all chromosomes is directly proportional to the number of RefSeq genes for each chromosome, except chromosome 20. (PDF 15 kb
Table S1. WGS of mouse strains mapped to human. Number of sequence reads from 3 mouse strains mapped...
Figure S2. Variability of allele depths. The known driver mutations are shown along with another foc...
The abundance and dynamics of copy number variants (CNVs) in mammalian genomes poses new challenges ...
Table S1. Rat exome-seq 500 flanking bp primer design for validation. (XLSX 20 kb
Table S2. PCR forward and reverse primer pairs for Sanger sequencing. (XLSX 10 kb
Table S1. Summary statistics for SNV and INDEL in various depths. Figure S1. Sequence coverage of th...
Abstract Background The rat genome was sequenced in 2004 with the aim to improve human health altere...
Frequency of rs200757797 and rs2740090 in the 1000 Genomes continental groups. (DOCX 13.4 kb
Systematic approach to study exome capture variability in exome-sequencing (A) Three-generation pedi...
Figure S1. The number of GATK-passed variants increase as cell input decreases. (PDF 39 kb
Table S1. Sequences used in BLAST analysis. Table S2. Detection of sex in sequenced rat genomes. Tab...
Figures S1â25. Data sources, methods overview, complete reporting of statistical analyses, and rep...
Additional comparisons of aCGH and exome-sequencing analyses of T-ALLs driven by Mps1 and p53 mutati...
We have determined the sequence of a 4-Mb interval on rat chromosome 20p12 that encompasses the rat ...
Table S1. Sequencing parameters for 3 samples with the highest and 3 samples with the lowest sequenc...
Table S1. WGS of mouse strains mapped to human. Number of sequence reads from 3 mouse strains mapped...
Figure S2. Variability of allele depths. The known driver mutations are shown along with another foc...
The abundance and dynamics of copy number variants (CNVs) in mammalian genomes poses new challenges ...
Table S1. Rat exome-seq 500 flanking bp primer design for validation. (XLSX 20 kb
Table S2. PCR forward and reverse primer pairs for Sanger sequencing. (XLSX 10 kb
Table S1. Summary statistics for SNV and INDEL in various depths. Figure S1. Sequence coverage of th...
Abstract Background The rat genome was sequenced in 2004 with the aim to improve human health altere...
Frequency of rs200757797 and rs2740090 in the 1000 Genomes continental groups. (DOCX 13.4 kb
Systematic approach to study exome capture variability in exome-sequencing (A) Three-generation pedi...
Figure S1. The number of GATK-passed variants increase as cell input decreases. (PDF 39 kb
Table S1. Sequences used in BLAST analysis. Table S2. Detection of sex in sequenced rat genomes. Tab...
Figures S1â25. Data sources, methods overview, complete reporting of statistical analyses, and rep...
Additional comparisons of aCGH and exome-sequencing analyses of T-ALLs driven by Mps1 and p53 mutati...
We have determined the sequence of a 4-Mb interval on rat chromosome 20p12 that encompasses the rat ...
Table S1. Sequencing parameters for 3 samples with the highest and 3 samples with the lowest sequenc...
Table S1. WGS of mouse strains mapped to human. Number of sequence reads from 3 mouse strains mapped...
Figure S2. Variability of allele depths. The known driver mutations are shown along with another foc...
The abundance and dynamics of copy number variants (CNVs) in mammalian genomes poses new challenges ...