<p>Sanger sequence validation of low expressed novel somatic SNVs for <i>FOXA1</i> in the BCT40 HER2 tumor sample. RNA-Seq sequence reads shown over Sanger sequence trace with mutation indicated by an arrow. </p
Over the last decade, the advent of high-throughput sequencing (HTS) has given us the ability to stu...
<p>Candidate mutations in 9 autosomal dominant and 4 autosomal recessive NSHL families were shown in...
All nine final selected variants carried by candidate modifier genes were validated by Sanger sequen...
<p>Sanger sequence validation of highly expressed novel somatic SNVs for <i>MRPL3</i> variant in the...
<p>Sanger sequencing validation of MPG eSNV in HER2 tumor. RNA-Seq reads shown over Sanger sequence ...
<p>Key: *Low confidence, Mutated Codon column-somatic mutation depicted in bold face.</p
<p>Of the filtered 41 candidates, 21 variants were confirmed by Sanger sequencing. Two examples are ...
<p>Five cases with matched tumor—blood samples are shown. Annotations in black letters are given for...
<p>Sanger sequencing validation of variants in the Simons Simplex Collection.</p
<p>Validation was performed using PCR on both genomic DNA and copy-DNA, followed by conventional San...
<p>Sanger sequencing of the results for the proband, parent and unaffected control at nucleotide pos...
Currently, the detection of single nucleotide variants (SNVs) from 10 x Genomics single-cell RNA seq...
<p>(A) Mapped reads of a Patient with RCMD loaded in the IGV browser (Version 2.3.34). <i>TET2</i> p...
Next-generation sequencing (NGS) has enabled the high-throughput discovery of germline and somatic m...
Over the last decade, the advent of high-throughput sequencing (HTS) has given us the ability to stu...
Over the last decade, the advent of high-throughput sequencing (HTS) has given us the ability to stu...
<p>Candidate mutations in 9 autosomal dominant and 4 autosomal recessive NSHL families were shown in...
All nine final selected variants carried by candidate modifier genes were validated by Sanger sequen...
<p>Sanger sequence validation of highly expressed novel somatic SNVs for <i>MRPL3</i> variant in the...
<p>Sanger sequencing validation of MPG eSNV in HER2 tumor. RNA-Seq reads shown over Sanger sequence ...
<p>Key: *Low confidence, Mutated Codon column-somatic mutation depicted in bold face.</p
<p>Of the filtered 41 candidates, 21 variants were confirmed by Sanger sequencing. Two examples are ...
<p>Five cases with matched tumor—blood samples are shown. Annotations in black letters are given for...
<p>Sanger sequencing validation of variants in the Simons Simplex Collection.</p
<p>Validation was performed using PCR on both genomic DNA and copy-DNA, followed by conventional San...
<p>Sanger sequencing of the results for the proband, parent and unaffected control at nucleotide pos...
Currently, the detection of single nucleotide variants (SNVs) from 10 x Genomics single-cell RNA seq...
<p>(A) Mapped reads of a Patient with RCMD loaded in the IGV browser (Version 2.3.34). <i>TET2</i> p...
Next-generation sequencing (NGS) has enabled the high-throughput discovery of germline and somatic m...
Over the last decade, the advent of high-throughput sequencing (HTS) has given us the ability to stu...
Over the last decade, the advent of high-throughput sequencing (HTS) has given us the ability to stu...
<p>Candidate mutations in 9 autosomal dominant and 4 autosomal recessive NSHL families were shown in...
All nine final selected variants carried by candidate modifier genes were validated by Sanger sequen...