Tracks available for Hydra Genome Browser:

Aligned ATAC-seq tracksAligned ATAC-seq reads as quantitative data in an x/y plot. ATAC-seq reads (replicate 1, 2, and 3) were generated for whole homeostatic Hydra. The Juliano_whole_peaks track is a consensus peak track consisting of all peaks that passed an IDR threshold of 0.1 for at least one pairwise comparison among the three biological replicates (Juliano_whole_rep1-3).
Aligned ATAC-seq reads from Murad et al. 2019 from adult tissues and regeneration time points 0-48h. Reads were aligned to the Hydra 2.0 genome using bowtie v. 1.2.
Aligned ChIP-seqAligned ChIP-seq reads from Murad et al. 2019 from whole Hydra, Hydra head and regeneration time points 0-24h. Reads were aligned to the Hydra 2.0 genome using bowtie v. 1.2.
Aligned RNA-seq tracksRNA-seq reads from Petersen et al. 2015 (Molecular Biology and Evolution) from time points 0-48h were aligned to the Hydra 2.0 genome using HISAT2. Aligned reads tracks display all aligned RNA-seq reads. BigWig XY tracks display the aligned RNA-seq reads as quantitative data in an x/y plot.
Aligned RNA-seq reads from Murad et al. 2019 from adult Hydra hypostome, tentacles, body column, budding zone and foot, also from regeneration time points 0-48h and budding stages 1-10. Reads were aligned to the Hydra 2.0 genome using bowtie v. 1.2.
Juliano_TrinityRNA-seq reads from Juliano et al. 2014 (PNAS) were assembled into Trinity transcripts. The Trinity assembled transcripts were aligned to the Hydra 2.0 genome using Splign.
Juliano_aepLRv2Transcripts from a transcriptome assembly for Hydra vulgaris AEP (38,749 transcripts) were aligned to the Hydra 2.0 genome using Splign.
Petersen_TrinityRNA-seq reads from Petersen et al. 2015 (Molecular Biology and Evolution) from time points 0–12 h were used to assemble a de novo transcriptome, which consists of 36,338 high quality transcripts. The Trinity assembled transcripts were aligned to the Hydra (2.0) genome using Splign.
AUGUSTUSHydra 2.0 gene models predicted using AUGUSTUS.
AUGUSTUS_unmaskedHydra 2.0 gene models predicted using AUGUSTUS with the unmasked genome.
FGENESHHydra 2.0 gene models predicted using FGENESH.
PASARNA-seq reads from Juliano et al. 2014 (PNAS) were assembled into Trinity transcripts. Transcripts were used to create gene structures based on spliced alignments with PASA.
Hydra1.0_JGIHydra 1.0 gene models (from JGI) aligned to the Hydra 2.0 genome assembly using Splign.
Hydra1.0_NCBIHydra 1.0 gene models (from NCBI) aligned to the Hydra 2.0 genome assembly using Splign.
BLASTP_augustus_vs_NCBI_nrBLASTP results from using AUGUSTUS protein models as queries against the NCBI nr protein database with an e-value cutoff of 1e-5.
BLASTP_augustus_vs_UniProtBLASTP results from using AUGUSTUS protein models as queries against the UniProt protein database with an e-value cutoff of 1e-5.
PASA_coding_regionsCandidate coding regions identified from PASA gene structures by TransDecoder.
AUGUSTUS_PFAMHydra 2.0 protein domains derived from PFAM HMMscans with an e-value cutoff of 1e-6 using the AUGUSTUS datasets.
6FRAMES_PFAMHydra 2.0 protein domains derived from PFAM HMMscans with an e-value cutoff of 1e-6 using the six-frame translations of the Hydra 2.0 genome.
Reference SequenceThe Hydra 2.0 genomic sequence and corresponding six-frame translations depicted when fully zoomed-in.
MASKGenomic regions that have been masked using RepeatMasker and RepeatModeler are highlighted in light blue.
SCFAssembled genomic scaffolds (SCF) appear as solid black tracks with intermittent gaps shaded bright pink.

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