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      Title: Detection of clinically relevant variants in the TP53 gene below 10% allelic frequency: A multicenter study by ERIC, the European Research Initiative on CLL
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        Title: INTRODUCTION
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        Title: METHODS
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          Title: Samples, cell lines, and patients
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          Title: Droplet digital polymerase chain reaction (ddPCR)
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          Title: Next-generation sequencing (NGS) methods
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          Title: Curation of TP53 variants
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          Title: Statistical analysis
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        Title: RESULTS
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          Title: Interlaboratory comparison of NGS methods
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          Title: The cumulative reliability of NGS methods for detecting low-frequent TP53 variants increased continuously with variant allele frequency
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          Title: Clinical impact of low-VAF TP53 variants
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        Title: DISCUSSION
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        Title: CONCLUSION
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    Subject: HemaSphere, doi:10.1002/hem3.70065
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   Type: CRC32
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   Type: MD5
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   Type: SHA-1
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   Type: SHA-256