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Include similarity of longest contigs between each sample
enhancementNew feature or requestNew feature or requestStatus: Open.#42 In folkehelseinstituttet/hcvtyper;Add de novo major and minor genotype to the summary
enhancementNew feature or requestNew feature or requestStatus: Open.#41 In folkehelseinstituttet/hcvtyper;Add distance to nearest reference
enhancementNew feature or requestNew feature or requestStatus: Open.#40 In folkehelseinstituttet/hcvtyper;Create run level reports and per sample reports
enhancementNew feature or requestNew feature or requestStatus: Open.#39 In folkehelseinstituttet/hcvtyper;Add RPM or RPKM for reporting
enhancementNew feature or requestNew feature or requestStatus: Open.#38 In folkehelseinstituttet/hcvtyper;Single reference per genotype
enhancementNew feature or requestNew feature or requestStatus: Open.#37 In folkehelseinstituttet/hcvtyper;Samplesheet script needs to correct sample names
enhancementNew feature or requestNew feature or requestStatus: Open.#33 In folkehelseinstituttet/hcvtyper;Vurdere nextclade for aa annotasjon
enhancementNew feature or requestNew feature or requestStatus: Open.#32 In folkehelseinstituttet/hcvtyper;De novo assembly for contamination or index hopping detection
enhancementNew feature or requestNew feature or requestStatus: Open.#30 In folkehelseinstituttet/hcvtyper;Check out new approach for reference genome selection and alignment
enhancementNew feature or requestNew feature or requestStatus: Open.#28 In folkehelseinstituttet/hcvtyper;Consider using a when block for minor mapping
enhancementNew feature or requestNew feature or requestStatus: Open.#26 In folkehelseinstituttet/hcvtyper;Consider removing optical duplicates in the reads
enhancementNew feature or requestNew feature or requestStatus: Open.#21 In folkehelseinstituttet/hcvtyper;