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PhyloCSF Novel M05
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PhyloCSF Candidate Coding Regions (PCCRs) Not In GENCODE vM5 Gene Set
PhyloCSF Novel M19
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PhyloCSF Candidate Coding Regions (PCCRs) Not In GENCODE vM19 Gene Set
PhyloCSF Novel M20
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PhyloCSF Candidate Coding Regions (PCCRs) Not In GENCODE vM20 Gene Set
PhyloCSF Novel M23
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PhyloCSF Candidate Coding Regions (PCCRs) Not In GENCODE vM23 Gene Set
PhyloCSF Novel M24
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PhyloCSF Candidate Coding Regions (PCCRs) Not In GENCODE vM24 Gene Set
PhyloCSF Novel M25
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PhyloCSF Candidate Coding Regions (PCCRs) Not In GENCODE vM25 Gene Set
Smoothed PhyloCSF
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Smoothed PhyloCSF
PhyloCSF-3
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Smoothed PhyloCSF Strand - Frame 3
PhyloCSF-2
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Smoothed PhyloCSF Strand - Frame 2
PhyloCSF-1
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Smoothed PhyloCSF Strand - Frame 1
PhyloCSF+3
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Smoothed PhyloCSF Strand + Frame 3
PhyloCSF+2
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Smoothed PhyloCSF Strand + Frame 2
PhyloCSF+1
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Smoothed PhyloCSF Strand + Frame 1
PhyloCSF Regions
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PhyloCSF approximate coding regions
PhyloCSF-3Regns
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PhyloCSF approximate coding regions, Strand -, Frame 3
PhyloCSF-2Regns
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PhyloCSF approximate coding regions, Strand -, Frame 2
PhyloCSF-1Regns
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PhyloCSF approximate coding regions, Strand -, Frame 1
PhyloCSF+3Regns
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PhyloCSF approximate coding regions, Strand +, Frame 3
PhyloCSF+2Regns
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PhyloCSF approximate coding regions, Strand +, Frame 2
PhyloCSF+1Regns
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PhyloCSF approximate coding regions, Strand +, Frame 1
Raw PhyloCSF
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Raw PhyloCSF
PhyloCSFraw-3
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Raw PhyloCSF Strand - Frame 3
PhyloCSFraw-2
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Raw PhyloCSF Strand - Frame 2
PhyloCSFraw-1
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Raw PhyloCSF Strand - Frame 1
PhyloCSFraw+3
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Raw PhyloCSF Strand + Frame 3
PhyloCSFraw+2
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Raw PhyloCSF Strand + Frame 2
PhyloCSFraw+1
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Raw PhyloCSF Strand + Frame 1
PhyloCSF Power
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Relative branch length of local alignment, a measure of PhyloCSF statistical power
Splice Predictions
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Splice Predictions
SplicePred-
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Splice Predictions For - Strand
SplicePred+
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Splice Predictions For + Strand
Base Position
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Chromosome position in bases. (Clicks here zoom in 3x)
p14
Fix Patches
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Reference Assembly Fix Patch Sequence Alignments
All Gaps
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All gaps of unknown nucleotides (N's), including AGP annotated gaps
p14
Alt Haplotypes
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Reference Assembly Alternate Haplotype Sequence Alignments
Assembly
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Assembly from Fragments
Chromosome Band
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Chromosome Bands Based On Microscopy
Clone Ends
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Mapping of clone libraries end placements
Contigs
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Contig fragments used in the assembly
Gap
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Gap Locations
GC Percent
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GC Percent in 5-Base Windows
GRC Incident
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GRC Incident Database
INSDC
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Accession at INSDC - International Nucleotide Sequence Database Collaboration
MGI QTL
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Mouse Genome Informatics Quantitative Trait Loci ***Lifted from NCBI 37 (mm9)***
Restr Enzymes
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Restriction Enzymes from REBASE
Short Match
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Perfect Matches to Short Sequence ()
UCSC liftOver mm39
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UCSC liftOver alignments to mm39
GENCODE VM23
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GENCODE VM23 Comprehensive Transcript Set (only Basic displayed by default)
updated
NCBI RefSeq
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RefSeq genes from NCBI
GENCODE Versions
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Container of all new and previous GENCODE releases
GENCODE VM9 (Ensembl 84)
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Gene Annotations from ENCODE/GENCODE Version M9 (Ensembl 84)
GENCODE VM11 (Ensembl 86)
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Gene Annotations from ENCODE/GENCODE Version M11 (Ensembl 86)
All GENCODE VM14
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All GENCODE annotations from VM14 (Ensembl 89)
All GENCODE VM16
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All GENCODE annotations from VM16 (Ensembl 91)
All GENCODE VM18
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All GENCODE annotations from VM18 (Ensembl 93)
All GENCODE VM22
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All GENCODE annotations from VM22 (Ensembl 97)
All GENCODE VM24
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All GENCODE annotations from VM24 (Ensembl 99)
All GENCODE VM25
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All GENCODE annotations from VM25 (Ensembl 100)
AUGUSTUS
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AUGUSTUS ab initio gene predictions v3.1
CCDS
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Consensus CDS
CRISPR 10K
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CRISPR/Cas9 Sp. Pyog. target sites (exons +/- 10,000 bp)
CRISPR Targets 10K
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CRISPR/Cas9 -NGG Targets (exons +/- 10,000 bp)
CRISPR Regions 10K
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Genome regions processed to find CRISPR/Cas9 target sites (exons +/- 10,000 bp)
CRISPR Targets
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CRISPR/Cas9 -NGG Targets, whole genome
Geneid Genes
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Geneid Gene Predictions
Genscan Genes
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Genscan Gene Predictions
MGC/ORFeome Genes
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MGC/ORFeome Full ORF mRNA Clones
ORFeome Clones
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ORFeome Collaboration Gene Clones
MGC Genes
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Mammalian Gene Collection Full ORF mRNAs
Old UCSC Genes
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Previous Version of UCSC Genes
Other RefSeq
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Non-Mouse RefSeq Genes
Pfam in UCSC Gene
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Pfam Domains in UCSC Genes
RetroGenes V6
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Retroposed Genes V6, Including Pseudogenes
SGP Genes
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SGP Gene Predictions Using Mouse/Human Homology
TOGA vs. hg38
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TOGA annotations using human/hg38 as reference
TransMap V5
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TransMap Alignments Version 5
TransMap ESTs
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TransMap EST Mappings Version 5
TransMap RNA
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TransMap GenBank RNA Mappings Version 5
TransMap RefGene
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TransMap RefSeq Gene Mappings Version 5
TransMap Ensembl
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TransMap Ensembl and GENCODE Mappings Version 5
tRNA Genes
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Transfer RNA Genes Identified with tRNAscan-SE
UCSC Alt Events
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Alternative Splicing, Alternative Promoter and Similar Events in UCSC Genes
UniProt
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UniProt SwissProt/TrEMBL Protein Annotations
Lens Patents
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Lens PatSeq Patent Document Sequences
UniProt Variants
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UniProt/SwissProt Amino Acid Substitutions
Spliced ESTs
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Mouse ESTs That Have Been Spliced
Mouse ESTs
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Mouse ESTs Including Unspliced
Mouse mRNAs
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Mouse mRNAs from GenBank
Other mRNAs
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Non-Mouse mRNAs from GenBank
ENCODE cCREs
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ENCODE Candidate Cis-Regulatory Elements (cCREs) combined from all cell types
Tabula Muris
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Single Cell FACS RNA-Seq of 44,779 cells from Tabula Muris
Splice Sites
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Tabula Muris single cell RNA-Seq splice sites
Genome Coverage
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Tabula Muris single cell RNA-Seq genome coverage
Cell expression
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Single Cell RNA-Seq Gene Expression from Tabula Muris
CpG Islands
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CpG Islands (Islands < 300 Bases are Light Green)
Unmasked CpG
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CpG Islands on All Sequence (Islands < 300 Bases are Light Green)
CpG Islands
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CpG Islands (Islands < 300 Bases are Light Green)
ENC+EPD Enhc-Gene
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Enhancer-gene map from ENCODE 3 (UCSD/Ren) with promoters from EPDnew
ENCODE Regulation
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Integrated Regulation from ENCODE
Open Chromatin
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Open chromatin in embryonic tissue (12 tissues, 8 ages) from ATAC-seq by ENCODE 3 (UCSD/Ren)
Histone Modifications
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Histone modifications in embryonic tissue (8 marks, 12 tissues, 8 ages) from ChIP-seq by ENCODE 3 (UCSD/Ren)
Chromatin State
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Chromatin state of embryonic tissue (12 tissues, 8 ages) from ENCODE 3 (UCSD/Ren)
EPDnew Promoters
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Promoters from EPDnew
FaceBase 24STypes
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FaceBase 24 Sample Types Averaged
FANTOM5
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FANTOM5: Mapped transcription start sites (TSS) and their usage
TSS activity (TPM)
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TSS activity per sample (TPM)
TSS activity (read counts)
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TSS activity per sample (read counts)
Max counts
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Max counts of CAGE reads
Total counts
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Total counts of CAGE reads
TSS peaks
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FANTOM5: DPI peak, robust set
JASPAR Transcription Factors
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JASPAR Transcription Factor Binding Site Database
ORegAnno
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Regulatory elements from ORegAnno
qPCR Primers
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Mouse (mm10) Whole Transcriptome qPCR Primers
RefSeq Func Elems
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NCBI RefSeq Functional Elements
ReMap ChIP-seq
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ReMap Atlas of Regulatory Regions
VISTA Enhancers
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VISTA Enhancers
Conservation
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Vertebrate Multiz Alignment & Conservation (60 Species)
ClinVar Lift
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Human ClinVar variants lifted to Mouse
Euarch Chain/Net
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Euarchontoglire Genomes, Chain and Net Alignments
Glires Chain/Net
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Glires Genomes, Chain and Net Alignments
Placental Chain/Net
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Placental Genomes, Chain and Net Alignments
Vertebrate Chain/Net
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Vertebrate Genomes, Chain and Net Alignments
Common SNPs(142)
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Simple Nucleotide Polymorphisms (dbSNP 142) Found in >= 1% of Samples
RepeatMasker
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Repeating Elements by RepeatMasker
Alternate strains
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Alternate mouse strain sequences
Alternate strains
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Alternate mouse strains, mapped to their corresponding reference genome location
Alignment
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Alternate mouse strains, alignments to reference genome
Interrupted Rpts
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Fragments of Interrupted Repeats Joined by RepeatMasker ID
Microsatellite
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Microsatellites - Di-nucleotide and Tri-nucleotide Repeats
Mouse SNPs
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Annotated SNPs from mouse strain comparison analysis
dbSNP Archive
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dbSNP Track Archive
Mult. SNPs(137)
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Simple Nucleotide Polymorphisms (dbSNP 137) That Map to Multiple Genomic Loci
Common SNPs(137)
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Simple Nucleotide Polymorphisms (dbSNP 137) Found in >= 1% of Samples
All SNPs(137)
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Simple Nucleotide Polymorphisms (dbSNP 137)
Mult. SNPs(138)
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Simple Nucleotide Polymorphisms (dbSNP 138) That Map to Multiple Genomic Loci
Common SNPs(138)
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Simple Nucleotide Polymorphisms (dbSNP 138) Found in >= 1% of Samples
All SNPs(138)
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Simple Nucleotide Polymorphisms (dbSNP 138)
Mult. SNPs(142)
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Simple Nucleotide Polymorphisms (dbSNP 142) That Map to Multiple Genomic Loci
All SNPs(142)
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Simple Nucleotide Polymorphisms (dbSNP 142)
EVA SNP
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Short Genetic Variants from European Variant Archive
RepeatMasker Viz.
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Detailed Visualization of RepeatMasker Annotations
Segmental Dups
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Duplications of >1000 Bases of Non-RepeatMasked Sequence
Simple Repeats
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Simple Tandem Repeats by TRF
WM + SDust
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Genomic Intervals Masked by WindowMasker + SDust