Biochemistry, Genetics and Molecular Biology
Photoreceptor Cell
100%
Myeloid
85%
Regulatory Sequence
66%
Binding Site
54%
Genomics
52%
Transcription Factors
49%
Allele
47%
Genetics
46%
Enhancer Region
44%
Genetic Variation
42%
Candidate Gene
42%
Genetic Divergence
42%
Homeodomain
40%
Exome Sequencing
38%
Whole Genome Sequencing
35%
Exome
32%
Laboratory Test
28%
Isoform
28%
Human Leukocyte Antigen
28%
Troponin
28%
Genome Sequencing
28%
Genome-Wide Association Study
28%
Cytogenetics
28%
Transcription
28%
Serum Response Factor
28%
Somatic Mutation
28%
Clonal Variation
28%
Clonality
28%
Thyroid Hormone Receptor
28%
Brain Development
28%
Ultrasound
28%
Decision Support System
28%
Thyroid Hormone
28%
Exon
25%
Single-Nucleotide Polymorphism
23%
Genetic Mechanism
23%
Gene Expression
22%
Homeobox
22%
Genome Wide Association Study
21%
Next Generation Sequencing
21%
Non-Coding RNA
20%
Evolution
20%
Proband
19%
DNA Sequence
17%
Electronic Medical Record
14%
Indel
14%
Oligonucleotide
14%
Minor Allele Frequency
14%
Copurification
14%
Monozygotic Twins
14%
Keyphrases
Cis-regulatory Elements
70%
Photoreceptor
65%
Photoreceptor Cells
47%
Homeodomain
47%
Type-specific
46%
Massively Parallel Reporter Assay
39%
Whole Genome Sequencing
38%
Binding Site
38%
Rod Photoreceptor
34%
Leukemia
32%
Cis-regulatory
32%
Enhancer Transcription
28%
Thrb
28%
Regulatory Base
28%
Genome-wide Association Study
28%
Hs-cTnT
28%
Human Leukocyte Antigen
28%
Exon
28%
Emergency Department Length of Stay
28%
Distinct Mechanism
28%
High-sensitivity Troponin
28%
Clinical Decision Support
28%
Cytogenetic Analysis
28%
Long Wavelength
28%
Chromatin Architecture
28%
Cone-rod Homeobox
28%
Divergence
28%
Transcript Isoforms
28%
Associated Genes
28%
Fallacies
28%
Clonality
28%
Tumor Samples
28%
Myeloid Cancer
28%
Thyroid Hormone Receptor
28%
Single-cell RNA Sequencing (scRNA-seq)
28%
Rapid Diagnostic Test
28%
Diagnostic Algorithm
28%
Laboratory Testing
28%
Infant Leukemia
28%
Non-synonymous Variations
28%
Group Reports
28%
PCTAIRE1
28%
Discharged Patients
28%
Secondary Acute Myeloid Leukemia (sAML)
28%
Allele-specific
28%
Genome Sequencing
28%
Children's Oncology Group
28%
Vertebrate Retina
28%
Epigenetic Analysis
28%
Nanopore Sequencing
28%