draft genome sequence Search Results


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Broad Institute Inc unpublished cichlid genome sequence data
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Integrated Genomics Inc draft sequence of gemmata sp. wa1-1
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Broad Institute Inc draft 7.6x sequence of the genome of boxer dogs
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BioResource International Inc draft genome sequence
Draft Genome Sequence, supplied by BioResource International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Broad Institute Inc draft genome sequences of six enterohepatic helicobacter species isolated from humans and one from rhesus macaques
Draft Genome Sequences Of Six Enterohepatic Helicobacter Species Isolated From Humans And One From Rhesus Macaques, supplied by Broad Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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China Center for Type Culture Collection draft genome sequence of comamonas jiangduensis strain yw1 t
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Elgavish Paramagnetics Inc draft genome sequence of the pathogenic bacterium vibrio vulnificus v252 biotype 1
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Broad Institute Inc draft genome sequence for monodelphis domestica
Pipeline for transcriptome assembly and analysis. A: single tissue samples were sequenced using NextGen sequencing technology to generate >200 million read pairs. B: 60 million randomly selected pairs were extracted and trimmed for adaptors and bases with quality score <30. C: reads were assembled using 2 methods: Trinity de novo assembly and alignment to the <t>Monodelphis</t> <t>domestica</t> NCBI reference genome (GCF_000002295.2 MonDom5) using TopHat and Cufflinks in the Tuxedo Suite. We tested parameters to determine which provides the most complete de novo assembly. D: de novo assembled contigs were aligned to the nucleotide RefSeq RNA database and to the protein Swiss-Prot database using BLASTn and BLASTx, respectively. The BLAST output against these databases was used to filter contigs that matched to mammals with an e-value <1e−4 and to annotate contigs with gene names. Using the Trinity provided module, we calculated the percent coverage of the top database match for each contig. E: from all assembled contigs, we utilized the various statistics to filter our assemblies, one whose amino acids matches identically to greater than or equal to 80% of their top database hit, and a second less stringent filter of contigs with at %Identity >70% and percent_hit_length >40% to include high-quality but partial transcript assemblies. F: the contigs in the filtered de novo assembly and the alignment to MonDom5 were quantified at the isoform and gene level using RSEM to generate counts, transcripts per million (TPM), and fragments per kilobase per million (FPKM). With the use of FPKM, the expression patterns were compared with published studies of rat kidney tubule expression.
Draft Genome Sequence For Monodelphis Domestica, supplied by Broad Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ANSES laboratories draft genome sequences of six ruminant coxiella burnetii isolates
Pipeline for transcriptome assembly and analysis. A: single tissue samples were sequenced using NextGen sequencing technology to generate >200 million read pairs. B: 60 million randomly selected pairs were extracted and trimmed for adaptors and bases with quality score <30. C: reads were assembled using 2 methods: Trinity de novo assembly and alignment to the <t>Monodelphis</t> <t>domestica</t> NCBI reference genome (GCF_000002295.2 MonDom5) using TopHat and Cufflinks in the Tuxedo Suite. We tested parameters to determine which provides the most complete de novo assembly. D: de novo assembled contigs were aligned to the nucleotide RefSeq RNA database and to the protein Swiss-Prot database using BLASTn and BLASTx, respectively. The BLAST output against these databases was used to filter contigs that matched to mammals with an e-value <1e−4 and to annotate contigs with gene names. Using the Trinity provided module, we calculated the percent coverage of the top database match for each contig. E: from all assembled contigs, we utilized the various statistics to filter our assemblies, one whose amino acids matches identically to greater than or equal to 80% of their top database hit, and a second less stringent filter of contigs with at %Identity >70% and percent_hit_length >40% to include high-quality but partial transcript assemblies. F: the contigs in the filtered de novo assembly and the alignment to MonDom5 were quantified at the isoform and gene level using RSEM to generate counts, transcripts per million (TPM), and fragments per kilobase per million (FPKM). With the use of FPKM, the expression patterns were compared with published studies of rat kidney tubule expression.
Draft Genome Sequences Of Six Ruminant Coxiella Burnetii Isolates, supplied by ANSES laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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draft genome sequences of six ruminant coxiella burnetii isolates - by Bioz Stars, 2026-08
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Progenesis Technologies LLC draft genome sequence of a mucoid isolate of pseudomonas aeruginosa strain c7447m
Pipeline for transcriptome assembly and analysis. A: single tissue samples were sequenced using NextGen sequencing technology to generate >200 million read pairs. B: 60 million randomly selected pairs were extracted and trimmed for adaptors and bases with quality score <30. C: reads were assembled using 2 methods: Trinity de novo assembly and alignment to the <t>Monodelphis</t> <t>domestica</t> NCBI reference genome (GCF_000002295.2 MonDom5) using TopHat and Cufflinks in the Tuxedo Suite. We tested parameters to determine which provides the most complete de novo assembly. D: de novo assembled contigs were aligned to the nucleotide RefSeq RNA database and to the protein Swiss-Prot database using BLASTn and BLASTx, respectively. The BLAST output against these databases was used to filter contigs that matched to mammals with an e-value <1e−4 and to annotate contigs with gene names. Using the Trinity provided module, we calculated the percent coverage of the top database match for each contig. E: from all assembled contigs, we utilized the various statistics to filter our assemblies, one whose amino acids matches identically to greater than or equal to 80% of their top database hit, and a second less stringent filter of contigs with at %Identity >70% and percent_hit_length >40% to include high-quality but partial transcript assemblies. F: the contigs in the filtered de novo assembly and the alignment to MonDom5 were quantified at the isoform and gene level using RSEM to generate counts, transcripts per million (TPM), and fragments per kilobase per million (FPKM). With the use of FPKM, the expression patterns were compared with published studies of rat kidney tubule expression.
Draft Genome Sequence Of A Mucoid Isolate Of Pseudomonas Aeruginosa Strain C7447m, supplied by Progenesis Technologies LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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draft genome sequence of a mucoid isolate of pseudomonas aeruginosa strain c7447m - by Bioz Stars, 2026-08
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Broad Institute Inc high-quality draft genome sequences of 28 enterococcus sp. isolates
Pipeline for transcriptome assembly and analysis. A: single tissue samples were sequenced using NextGen sequencing technology to generate >200 million read pairs. B: 60 million randomly selected pairs were extracted and trimmed for adaptors and bases with quality score <30. C: reads were assembled using 2 methods: Trinity de novo assembly and alignment to the <t>Monodelphis</t> <t>domestica</t> NCBI reference genome (GCF_000002295.2 MonDom5) using TopHat and Cufflinks in the Tuxedo Suite. We tested parameters to determine which provides the most complete de novo assembly. D: de novo assembled contigs were aligned to the nucleotide RefSeq RNA database and to the protein Swiss-Prot database using BLASTn and BLASTx, respectively. The BLAST output against these databases was used to filter contigs that matched to mammals with an e-value <1e−4 and to annotate contigs with gene names. Using the Trinity provided module, we calculated the percent coverage of the top database match for each contig. E: from all assembled contigs, we utilized the various statistics to filter our assemblies, one whose amino acids matches identically to greater than or equal to 80% of their top database hit, and a second less stringent filter of contigs with at %Identity >70% and percent_hit_length >40% to include high-quality but partial transcript assemblies. F: the contigs in the filtered de novo assembly and the alignment to MonDom5 were quantified at the isoform and gene level using RSEM to generate counts, transcripts per million (TPM), and fragments per kilobase per million (FPKM). With the use of FPKM, the expression patterns were compared with published studies of rat kidney tubule expression.
High Quality Draft Genome Sequences Of 28 Enterococcus Sp. Isolates, supplied by Broad Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Pipeline for transcriptome assembly and analysis. A: single tissue samples were sequenced using NextGen sequencing technology to generate >200 million read pairs. B: 60 million randomly selected pairs were extracted and trimmed for adaptors and bases with quality score <30. C: reads were assembled using 2 methods: Trinity de novo assembly and alignment to the Monodelphis domestica NCBI reference genome (GCF_000002295.2 MonDom5) using TopHat and Cufflinks in the Tuxedo Suite. We tested parameters to determine which provides the most complete de novo assembly. D: de novo assembled contigs were aligned to the nucleotide RefSeq RNA database and to the protein Swiss-Prot database using BLASTn and BLASTx, respectively. The BLAST output against these databases was used to filter contigs that matched to mammals with an e-value <1e−4 and to annotate contigs with gene names. Using the Trinity provided module, we calculated the percent coverage of the top database match for each contig. E: from all assembled contigs, we utilized the various statistics to filter our assemblies, one whose amino acids matches identically to greater than or equal to 80% of their top database hit, and a second less stringent filter of contigs with at %Identity >70% and percent_hit_length >40% to include high-quality but partial transcript assemblies. F: the contigs in the filtered de novo assembly and the alignment to MonDom5 were quantified at the isoform and gene level using RSEM to generate counts, transcripts per million (TPM), and fragments per kilobase per million (FPKM). With the use of FPKM, the expression patterns were compared with published studies of rat kidney tubule expression.

Journal: American Journal of Physiology - Renal Physiology

Article Title: The transcriptome of the Didelphis virginiana opossum kidney OK proximal tubule cell line

doi: 10.1152/ajprenal.00228.2017

Figure Lengend Snippet: Pipeline for transcriptome assembly and analysis. A: single tissue samples were sequenced using NextGen sequencing technology to generate >200 million read pairs. B: 60 million randomly selected pairs were extracted and trimmed for adaptors and bases with quality score <30. C: reads were assembled using 2 methods: Trinity de novo assembly and alignment to the Monodelphis domestica NCBI reference genome (GCF_000002295.2 MonDom5) using TopHat and Cufflinks in the Tuxedo Suite. We tested parameters to determine which provides the most complete de novo assembly. D: de novo assembled contigs were aligned to the nucleotide RefSeq RNA database and to the protein Swiss-Prot database using BLASTn and BLASTx, respectively. The BLAST output against these databases was used to filter contigs that matched to mammals with an e-value <1e−4 and to annotate contigs with gene names. Using the Trinity provided module, we calculated the percent coverage of the top database match for each contig. E: from all assembled contigs, we utilized the various statistics to filter our assemblies, one whose amino acids matches identically to greater than or equal to 80% of their top database hit, and a second less stringent filter of contigs with at %Identity >70% and percent_hit_length >40% to include high-quality but partial transcript assemblies. F: the contigs in the filtered de novo assembly and the alignment to MonDom5 were quantified at the isoform and gene level using RSEM to generate counts, transcripts per million (TPM), and fragments per kilobase per million (FPKM). With the use of FPKM, the expression patterns were compared with published studies of rat kidney tubule expression.

Article Snippet: However, the genomic sequence for D. virginiana is not available and although a draft genome sequence for the opossum Monodelphis domestica (sequenced in 2012 by the Broad Institute) exists, transcripts sequenced from both species show significant divergence.

Techniques: Sequencing, Expressing

Analysis of BLAST results. Contigs assembled using Trinity for the Didelphis virginiana at kmer coverage settings 3 and 10 were aligned to the RefSeq RNA database using BLASTn (A and B) and to the Swiss-Prot database using BLASTx (C and D). Of the total contigs constructed by Trinity in each assembly, the number of contigs with a BLAST alignment to each respective database is shown above each pie chart. Left: number of contigs from matches with an e-value >1e−4 (blue-region) or e-value ≤1e−4 (green-region). Right: the contigs with e-value ≤1e−4 (green-region) are further broken down into their species distribution, specifically highlighting matches to M. domestica, Homo sapiens, and Mus musculus (human and mouse), other mammals, or those that did not have a top hit to mammals. A and B also denote the number of matches to the predicted M. domestica genome since mostly predicted transcripts are present in the RefSeq RNA database.

Journal: American Journal of Physiology - Renal Physiology

Article Title: The transcriptome of the Didelphis virginiana opossum kidney OK proximal tubule cell line

doi: 10.1152/ajprenal.00228.2017

Figure Lengend Snippet: Analysis of BLAST results. Contigs assembled using Trinity for the Didelphis virginiana at kmer coverage settings 3 and 10 were aligned to the RefSeq RNA database using BLASTn (A and B) and to the Swiss-Prot database using BLASTx (C and D). Of the total contigs constructed by Trinity in each assembly, the number of contigs with a BLAST alignment to each respective database is shown above each pie chart. Left: number of contigs from matches with an e-value >1e−4 (blue-region) or e-value ≤1e−4 (green-region). Right: the contigs with e-value ≤1e−4 (green-region) are further broken down into their species distribution, specifically highlighting matches to M. domestica, Homo sapiens, and Mus musculus (human and mouse), other mammals, or those that did not have a top hit to mammals. A and B also denote the number of matches to the predicted M. domestica genome since mostly predicted transcripts are present in the RefSeq RNA database.

Article Snippet: However, the genomic sequence for D. virginiana is not available and although a draft genome sequence for the opossum Monodelphis domestica (sequenced in 2012 by the Broad Institute) exists, transcripts sequenced from both species show significant divergence.

Techniques: Construct