Publication date
August 2022
DOIAbstract
This minor feature improvement now shows cell line IDs while listing all available mutations using list_available_mutations()
This minor feature improvement now shows cell line IDs while listing all available mutations using list_available_mutations()
Mutations identified using next generation sequencing as stratified by the European society of medic...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
Implementation of GiniClust2, a tool created to discover rare and common cell types in single-cell g...
VariantIterator can now skip neutral or selected mutations during traversal. Documentation updates
Updated to include: Table of alleles for calling AMR mutations Table of alleles for calling genotyp...
GINIR package name has now changed to GRETA (Genetic inteRaction and EssenTially mApper) GINI_screen...
Data for Izzilab/pancancer-matrisome-mutations: pancancer matrisome mutations v.0
<p>Specific mutations within each clade are indicated. Fixed mutations, systematically present in al...
Since 1989, about 570 different p53 mutations have been identified in more than 8000 human cancers. ...
New features: Added flag to indicate if a mutation mentioned used 1-letter code. This can be usef...
<p>Variant caller sensitivity for detecting the manually curated mutations for SNVs and indels are s...
<p>For each target gene, the total number of mutations, total number of germline-transmitting founde...
Page 1 contains the nucleotide substitutions observed on each evolved lineage. Page 2 contains a sc...
Background—Evolution depends on mutations: rare errors in the transmission of genetic information. E...
Stars indicate mutations (top); red bars indicate changepoints (middle); green and purple lines indi...
Mutations identified using next generation sequencing as stratified by the European society of medic...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
Implementation of GiniClust2, a tool created to discover rare and common cell types in single-cell g...
VariantIterator can now skip neutral or selected mutations during traversal. Documentation updates
Updated to include: Table of alleles for calling AMR mutations Table of alleles for calling genotyp...
GINIR package name has now changed to GRETA (Genetic inteRaction and EssenTially mApper) GINI_screen...
Data for Izzilab/pancancer-matrisome-mutations: pancancer matrisome mutations v.0
<p>Specific mutations within each clade are indicated. Fixed mutations, systematically present in al...
Since 1989, about 570 different p53 mutations have been identified in more than 8000 human cancers. ...
New features: Added flag to indicate if a mutation mentioned used 1-letter code. This can be usef...
<p>Variant caller sensitivity for detecting the manually curated mutations for SNVs and indels are s...
<p>For each target gene, the total number of mutations, total number of germline-transmitting founde...
Page 1 contains the nucleotide substitutions observed on each evolved lineage. Page 2 contains a sc...
Background—Evolution depends on mutations: rare errors in the transmission of genetic information. E...
Stars indicate mutations (top); red bars indicate changepoints (middle); green and purple lines indi...
Mutations identified using next generation sequencing as stratified by the European society of medic...
The Human Gene Mutation Database (HGMD) constitutes a comprehensive core collection of data on germ-...
Implementation of GiniClust2, a tool created to discover rare and common cell types in single-cell g...
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