Publications:

AMLVaran: a software approach to implement variant analysis of targeted NGS sequencing data in an oncological care setting.

Bmc Medical Genomics

Wünsch, Christian C; Banck, Henrik H; Müller-Tidow, Carsten C; Dugas, Martin M

Publication Date: 2020-02-04

Variant appearance in text: TP53: 961A>C; K321Q

PubMed Link: 32019565

Variant Present in the following documents:

• 12920_2020_668_MOESM5_ESM.xls, sheet 1
• 12920_2020_668_MOESM6_ESM.xls, sheet 1

View BVdb publication page

appreci8: a pipeline for precise variant calling integrating 8 tools.

Bioinformatics (Oxford, England)

Sandmann, Sarah S; Karimi, Mohsen M; de Graaf, Aniek O AO; Rohde, Christian C; Göllner, Stefanie S; Varghese, Julian J; Ernsting, Jan J; Walldin, Gunilla G; van der Reijden, Bert A BA; Müller-Tidow, Carsten C; Malcovati, Luca L; Hellström-Lindberg, Eva E; Jansen, Joop H JH; Dugas, Martin M

Publication Date: 2018-12-15

Variant appearance in text: TP53: 961A>C; Lys321Gln

PubMed Link: 29945233

Variant Present in the following documents:

• bty518_supplementary_data_s4.xlsx, sheet 9
• bty518_supplementary_data_s3.xlsx, sheet 9
• bty518_supplementary_data_s4.xlsx, sheet 8
• bty518_supplementary_data_s3.xlsx, sheet 8

View BVdb publication page

iFish: predicting the pathogenicity of human nonsynonymous variants using gene-specific/family-specific attributes and classifiers.

Scientific Reports

Wang, Meng M; Wei, Liping L

Publication Date: 2016-08-16

Variant appearance in text: TP53: K321Q

PubMed Link: 27527004

Variant Present in the following documents:

• srep31321-s5.xls, sheet 1

View BVdb publication page

Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes.

Molecular Cancer Research : Mcr

Monti, Paola P; Perfumo, Chiara C; Bisio, Alessandra A; Ciribilli, Yari Y; Menichini, Paola P; Russo, Debora D; Umbach, David M DM; Resnick, Michael A MA; Inga, Alberto A; Fronza, Gilberto G

Publication Date: 2011-03

Variant appearance in text: p53: Lys321Gln

PubMed Link: 21343334

Variant Present in the following documents:

• Main text

View BVdb publication page