Biochemistry, Genetics and Molecular Biology
CRISPR
100%
Enhancer Region
55%
Cancer Cell
50%
Gene Expression
46%
Epigenetics
43%
Chromatin Immunoprecipitation
42%
Kinase
41%
Phosphotransferase
41%
Cas9
34%
Genomics
34%
Methylation
32%
CRISPR/Cas9
32%
Germline
31%
Germ Cell
31%
Small Molecule
31%
Epigenome
31%
Binding Site
29%
Transcription Factors
28%
Genetics
28%
Transcription Factor RUNX
27%
Motion
27%
Reprogramming
27%
Clinical Trial
27%
High Throughput Sequencing
27%
Gene Expression Profiling
26%
Myeloid
22%
Histone Modification
21%
Dynamics
21%
RNA
21%
RNA Sequence
20%
Gene Mutation
20%
Single-Nucleotide Polymorphism
20%
Guide RNA
19%
Somatic Mutation
19%
Epigenomics
18%
Metabolic Pathway
18%
Epigenetics
18%
DNA Methylation
18%
Histone
18%
Tumor Suppressor Protein
17%
Protein-DNA Interaction
17%
Stem Cell
17%
Deep Sequencing
16%
Lysine
16%
Polycomb Repressive Complex 2
15%
Methyltransferase
15%
Gene Mapping
15%
Complement Factor B
15%
Exome Sequencing
15%
Whole Genome Sequencing
15%
Keyphrases
Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)
72%
Transcription Factor
51%
Chromatin Immunoprecipitation (ChIP)
46%
Adenomyosis
41%
Gene Expression
36%
Factor-driven
34%
Cas9 Protein
33%
Ovarian Cancer
31%
Chromatin State
31%
Whole Genome
30%
Binding Site
29%
Transcriptional Program
29%
Chromatin
27%
Polycomb Repressive Complex 2 (PRC2)
27%
Functional Variants
27%
Small Molecule Inhibitors
27%
Genome-wide Analysis
27%
Enhancer Activity
27%
Pancreatic Cancer
27%
Single Guide RNA (sgRNA)
27%
Glioma Risk
27%
Leiomyoma
27%
High-throughput Sequencing
25%
Cancer Cells
25%
NF-B
25%
ASXL1
23%
Histone Modification
22%
Phosphorylation
22%
DCas9
22%
CRISPR Screening
22%
Uterine Fibroids
21%
Genome Sequencing
21%
Super-enhancer
20%
Epigenome Editing
20%
Mammalian Cells
19%
Trimethylation
18%
CRISPR Tool
18%
Gene Regulation
18%
Gene Editing
18%
Endometriosis
18%
Genome Editing
18%
Clinical Trials
18%
Chemoresistance
17%
Pancreatic Ductal Adenocarcinoma
17%
Prostate Cancer Cells
17%
H3K79me2
17%
Drug Target
17%
Transcriptional Changes
17%
Cell number
17%
Genetic Variants
16%