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Comment: Comment: Commercial software for genomics / NGS / bioinformatics
21 months ago by liorglic ★ 1.4k
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0
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752
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Comment: Comment: SNP calling from plant whole genome assemblies
22 months ago by liorglic ★ 1.4k
1
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0
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2.2k
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Comment: Comment: convert csv to fasta format using python
2.0 years ago by liorglic ★ 1.4k
0
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1
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710
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Comment: Comment: URGENT : GC @5,20,50 : Fraction of GC content in the bases around the variant po
2.0 years ago by liorglic ★ 1.4k
0
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0
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717
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Comment: Comment: Sort the fasta sequences based on the desired amino acid content
2.1 years ago by liorglic ★ 1.4k
1
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1
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887
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Comment: Comment: Is it possible to create a phylogenetic tree based on 10 proteins per organism
2.1 years ago by liorglic ★ 1.4k
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1
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887
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Comment: Comment: Is it possible to create a phylogenetic tree based on 10 proteins per organism
2.1 years ago by liorglic ★ 1.4k
0
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0
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577
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Comment: Comment: Over view informations about my genomes
2.1 years ago by liorglic ★ 1.4k
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0
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1.1k
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Comment: Comment: vg for gene presence-absence analysis
2.1 years ago by liorglic ★ 1.4k
0
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1
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712
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Comment: Comment: DGE - command line alternatives to R packages?
2.2 years ago by liorglic ★ 1.4k
0
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0
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767
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Comment: Comment: What metrics to use for comparing alignment-based methods and variant calling fo
2.2 years ago by liorglic ★ 1.4k
0
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0
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647
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Comment: Comment: Genotypes in vcf files
2.3 years ago by liorglic ★ 1.4k
1
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1
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1.3k
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Comment: Comment: Filter isoforms before or after genome annotation
2.3 years ago by liorglic ★ 1.4k
0
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1
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1.3k
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Comment: Comment: Plant de novo genome assembly of illumina reads on linux
2.3 years ago by liorglic ★ 1.4k
1
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1
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1.3k
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Comment: Comment: Filter isoforms before or after genome annotation
2.3 years ago by liorglic ★ 1.4k
0
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0
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758
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Comment: Comment: Is there any way to determine if a gene is due to contamination?
2.3 years ago by liorglic ★ 1.4k
0
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0
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4.3k
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Comment: Comment: Trouble with bedtools getfasta
2.3 years ago by liorglic ★ 1.4k
0
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1
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4.3k
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Comment: Comment: Trouble with bedtools getfasta
2.3 years ago by liorglic ★ 1.4k
0
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1
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4.3k
views
Comment: Comment: Trouble with bedtools getfasta
updated 2.3 years ago by 44k • written 2.3 years ago by ★ 1.4k
0
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1
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860
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Comment: Comment: Bam in python
2.3 years ago by liorglic ★ 1.4k
0
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0
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429
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Comment: Comment: Incorporate SNP/Indel and generate new sequence from original reference gene seq
2.3 years ago by liorglic ★ 1.4k
0
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1
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547
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Comment: Comment: studying similarity
2.3 years ago by liorglic ★ 1.4k
1
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0
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1.2k
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Comment: Comment: How can I extract part of the DNA sequences that align to a specific region in t
2.3 years ago by liorglic ★ 1.4k
0
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1
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1.1k
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Comment: Comment: How is genome coverage / depth is determined?
2.3 years ago by liorglic ★ 1.4k
1
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2
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1.1k
views
Comment: Comment: How is genome coverage / depth is determined?
2.3 years ago by liorglic ★ 1.4k
1
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1
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1.4k
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Comment: Comment: Merging two sets of NGS reads
2.3 years ago by liorglic ★ 1.4k
0
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0
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1.6k
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Comment: Comment: Unsupervised hierarchical clustering of DEG in Rstudio
2.3 years ago by liorglic ★ 1.4k
0
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0
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804
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Comment: Comment: String values replace in python data frame
2.3 years ago by liorglic ★ 1.4k
0
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1
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1.4k
views
Comment: Comment: Merging two sets of NGS reads
2.3 years ago by liorglic ★ 1.4k
0
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1
reply
1.6k
views
Comment: Comment: Unsupervised hierarchical clustering of DEG in Rstudio
2.3 years ago by liorglic ★ 1.4k
0
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1
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1.6k
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Comment: Comment: Unsupervised hierarchical clustering of DEG in Rstudio
2.3 years ago by liorglic ★ 1.4k
0
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0
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875
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Comment: Comment: Iso-seq mapping and annotation
2.3 years ago by liorglic ★ 1.4k
0
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0
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831
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Comment: Comment: how to discover the dissimilar regions in alignment using pyhton?
2.3 years ago by liorglic ★ 1.4k
0
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1
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1.7k
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Comment: Comment: How to solve Non-unique top level ID error in Maker annotation pipeline ?
2.3 years ago by liorglic ★ 1.4k
0
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0
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895
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Comment: Comment: Paired-end reads
2.3 years ago by liorglic ★ 1.4k
1
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0
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4.7k
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Comment: Comment: It seems that 'fastuniq' does not support fq.gz files. How to solve this except
2.4 years ago by liorglic ★ 1.4k
0
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0
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1.0k
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Comment: Comment: Clumpify on multiple files
2.4 years ago by liorglic ★ 1.4k
0
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1
reply
788
views
Comment: Comment: Data sets of WGS + disease phenotypes?
2.4 years ago by liorglic ★ 1.4k
1
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1
reply
563
views
Comment: Comment: Are RFLP and ITS both molecular markers?
2.4 years ago by liorglic ★ 1.4k
0
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0
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2.1k
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Comment: Comment: Snakemake command line arguments
2.4 years ago by liorglic ★ 1.4k
0
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0
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626
views
Comment: Comment: Count number of values in a nested dictionary
2.4 years ago by liorglic ★ 1.4k
0
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1
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1.1k
views
Comment: Comment: asterisk in phylip file
2.4 years ago by liorglic ★ 1.4k
0
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0
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573
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Comment: Comment: Genome variants - regional distribution analysis
2.4 years ago by liorglic ★ 1.4k
0
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0
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1.1k
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Comment: Comment: Is there a way to change only the header of a fasta file?
2.4 years ago by liorglic ★ 1.4k
1
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1
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1.1k
views
Comment: Comment: Is there a way to change only the header of a fasta file?
2.4 years ago by liorglic ★ 1.4k
0
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0
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1.4k
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Comment: Comment: Generating Depth of Coverage files from vcf.
2.4 years ago by liorglic ★ 1.4k
0
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1
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1.7k
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Comment: Comment: How to plot depth coverage plot?
2.5 years ago by liorglic ★ 1.4k
0
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0
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934
views
Comment: Comment: BAM - number of mapping positions per read
2.5 years ago by liorglic ★ 1.4k
0
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1
reply
949
views
Comment: Comment: Script for chromosome features
2.6 years ago by liorglic ★ 1.4k
0
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1
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3.5k
views
Comment: Comment: Simplify annotation file by collapsing gene isoforms into a single annotation pe
2.6 years ago by liorglic ★ 1.4k
158 results • Page 2 of 4
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